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Chemical Structure| 36743-66-5 Chemical Structure| 36743-66-5

Structure of 36743-66-5

Chemical Structure| 36743-66-5

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Product Details of [ 36743-66-5 ]

CAS No. :36743-66-5
Formula : C4H9Cl2NO
M.W : 158.03
SMILES Code : N=C(OCC)CCl.[H]Cl
MDL No. :MFCD10697958

Safety of [ 36743-66-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501

Application In Synthesis of [ 36743-66-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 36743-66-5 ]

[ 36743-66-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 36743-66-5 ]
  • [ 95-55-6 ]
  • [ 41014-43-1 ]
YieldReaction ConditionsOperation in experiment
95% In dichloromethane; at 0 - 20℃; B. To a stirred suspension of 2-aminophenol (365 mg, 3.35 mmol) in dichloromethane (7 mL) at 00C was added compound ethyl 2-chloroacetimidate hydrochloride (798 mg, 5.05 mmol) portion-wise. After 1 hour 25 min. at 00C, the mixture was stirred at ambient temperature overnight. The mixture was filtered through Celite and the filtrate was concentrated. The residue was purified by column (hexanes/EtOAc, 7/3) to afford 2-(chloromethyl)benzoxazole as a pale oil (533 mg, 95%).
86.5% With acetic acid; In dichloromethane; at 0 - 20℃; for 1.41667h; To a solution of 2-aminophenol (3.76 g,34.5 mmol) in methylene chloride at 0 C was added ethyl chloroacetimidate hydrochloride (7.98 g,50.5 mmol). After 85 min, the reaction mixture was allowed to warm to room temperature, while beingstirred overnight. The mixture was filtered over diatomite and concentrated to oil under reducedpressure. The resulting residue was purified by column chromatography on silica gel (petroleumether/acetone, 10:1 v:v) to obtain compound 3 as a white solid (5.00 g, 86.5%). m.p., 152-154 C;MS (+ESI) m/z 168.05 [M + H]+
75% at 0℃; for 6h; General procedure: General Method B: To the solution of substituted 2-aminophenol (1.0 equiv.) or substituted benzene-1, 2-diamine(1.0 equiv.) in DCM (or CH3OH), Int 1 (1.5 equiv.) was added and stirred at 0C overnight. The mixture was filteredwith celite. The filtrate was concentrated, purified by silica gel chromatography (EtOAc:hexane = 1:1) to afford thedesired products.
3.99 g (65%) In ethanol; dichloromethane; Step 1) Preparation of 2-(Chloromethyl)benzoxazole A mixture of o-aminophenol (4.00 g, 36.6 mmol) and ethyl chloroacetimidate hydrochloride (8.68 g, 54.98 mmol) in ethanol (55 mL) was heated at reflux for 18 hours. The reaction mixture was cooled to room temperature and vacuum filtered. The filtrate was concentrated in vacuo, diluted with dichloromethane and filtered again. The methylene chloride filtrate was dried (MgSO4) and concentrated to afford 3.99 g (65%) of product as a brown oil which was used directly in the next step. 1 H NMR (CDCl3): delta7.73 (m, 1H, ArH), 7.56 (m, 1H, ArH), 7.38 (m, 2H, ArH), 4.76 (s, 2H, CH2 Cl).
3.99 g (65%) In ethanol; dichloromethane; Step 1) Preparation of 2-(Chloromethyl)benzoxazole A mixture of o-aminophenol (4.00 g, 36.6 mmol) and ethyl chloroacetimidate hydrochloride (8.68 g, 54.98 mmol) in ethanol (55 mL) was heated at reflux for 18 hours. The reaction mixture was cooled to room temperature and vacuum filtered. The filtrate was concentrated in vacuo, diluted with methylene chloride and filtered again. The methylene chloride filtrate was dried (MgSO4) and concentrated to afford 3.99 g (65%) of product as a brown oil which was used directly in the next step. 1 H NMR (CDCl3): delta7.73 (m, 1H, ArH), 7.56 (m, 1H, ArH), 7.38 (m, 2H, ArH), 4.76 (s, 2H, CH2 Cl).

  • 2
  • N<SUP>4</SUP>-semicarbazide hydrochloride [ No CAS ]
  • [ 36743-66-5 ]
  • [ 252742-72-6 ]
YieldReaction ConditionsOperation in experiment
62% In ethanol; at 20℃; for 35h; 60.4 g (0.8 mol) of chloroacetonitrile and 36.8 g of ethanol (water content 0.06percent) were placed in a magnetic stirring reactor.(0.8 mol) and 400 g of dichloromethane, cooled to 5 ° C, controlled to slowly and uniformly pass 32 g (0.88 mol) of dry HCl gas below this temperature. After the completion of the aeration, the reaction was stirred for 10 h, and a large number of white needles were observed. Crystal formationThe filter residue was filtered to obtain iminochloroethyl ethyl ether hydrochloride.300 g of ethanol was placed in the reaction vessel, and the temperature was raised to 50 ° C with stirring.Then add the iminochloroethyl methyl ether hydrochloride 128g,And maintaining the reaction at 45 ° C for 6 hours; The reaction solution was stirred and cooled to -5 ° C, and suction filtered; the filtrate was stirred and heated to 40 ° C.Adding 19.5 g (0.14 mol) of semicarbazide hydrochloride,And stirring the reaction at this temperature for 35 hours; the reaction solution was filtered,The filtrate was concentrated to dryness under reduced pressure at 50 ° C to 50 ° C.The obtained solid was added to 150 g of acetone, and stirred under reflux for 30 min.The filtrate was filtered while hot, and the filtrate was cooled and crystallized at -5 ° C.Made of white fine needle crystals,Is 3-chloromethyl-1,2,4-triazolin-5-one, filtered,Drying at 55 ° C under vacuum to obtain a white powdery solid3-chloromethyl-1,2,4-triazolin-5-one 11.5g,The total molar yield (based on semicarbazide hydrochloride) was 62percent and the HPLC purity was 99.5percent.
 

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