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Chemical Structure| 5121-00-6 Chemical Structure| 5121-00-6

Structure of 5121-00-6

Chemical Structure| 5121-00-6

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Product Details of [ 5121-00-6 ]

CAS No. :5121-00-6
Formula : C12H9ClO
M.W : 204.65
SMILES Code : O=C(Cl)CC1=C2C=CC=CC2=CC=C1
MDL No. :MFCD00175852
InChI Key :DSVAZLXLRDXHKO-UHFFFAOYSA-N
Pubchem ID :2795386

Safety of [ 5121-00-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 5121-00-6 ]

* 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 [ 5121-00-6 ]

[ 5121-00-6 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 5121-00-6 ]
  • [ 86-86-2 ]
YieldReaction ConditionsOperation in experiment
72% With ammonium hydroxide; In tetrahydrofuran; at 0 - 20℃; for 0.166667h; 1-naphthaleneacetic acid (93.5 mg, 0.50 mmol) was added to methylene chloride (0.8 mL)And a catalytic amount of DMF were added and while stirring,Further oxalyl chloride (135.6 mg, 1.00 mmol, 2.00 eq.) Was added dropwise,Followed by stirring at room temperature for 15 minutes. After concentrating the resulting solution under vacuum,Was dissolved in tetrahydrofuran (0.8 mL).Ammonia water (28%, 450.4 mg, 7.50 mmol, 15.0 eq.) At 0 C. was added to the solution,It was then stirred at room temperature for 10 minutes. After concentrating the resulting solution under vacuum,Silica gel column chromatography (chloroform / methanol(10/1, Rf = 0.50)) to obtain the target substance (Y-015) as a white solid (yield 72%).
With 1,1,1,3,3,3-hexamethyl-disilazane; In dichloromethane; at 0 - 20℃; General procedure: To an over-dried 100 mL three-necked flask, the carboxylic acid (10 mmol), DMF (5 drops) and DCM (30 mL) were added under a N2 atmosphere. Oxalyl chloride (1.0 mL, 12 mmol) was added dropwise at 0 C resulting in vigorous bubbling. The mixture was stirred for 3 h at room temperature, and the solvent was then removed in vacuo. The resulting acid chloride was used immediately without further purification. To a solution of the acid chloride in DCM (30 mL) ,a solution of 1,1,1,3,3,3-hexamethyldisilazane (30 mmol) in DCM (10 mL) was added dropwise at 0 C, and the solution was then allowed to warm to room temperature. After stirring overnight, the reaction system was quenched with 1 M HCl aq. and saturated aqueous NH4Cl (excess amount) and the organic layer was separated. The aqueous layer was extracted with DCM (2x15 mL). The combined organic layers were washed with saturated aqueous NH4Cl (30 mL) and brine (30 mL), dried over MgSO4, filtered and evaporated in vacuo. The resulting crude material was purified by recrystallization from EtOAc and hexane. The resulting product (5 mmol), 8-bromomethylquinoline (6 mmol), Al2O3 (50 mmol), KOH (25 mmol) and dioxane (30 mL) were added to an over-dried 100 mL three-necked flask. The mixture was stirred for 8 h at 60 C and then was filtered through a celite pad. The filtrate was washed with H2O (30 mL) and the organic layer was separated. The aqueous layer was extracted with EtOAc (2x15 mL). The combined organic layers were washed with brine (15 mL), dried over anhydrous Na2SO4, filtrated and evaporated in vacuo. The resulting crude amide was purified by column chromatography on silica gel (eluent: hexane/EtOAc = 1/1).
  • 2
  • [ 5121-00-6 ]
  • [ 932-32-1 ]
  • [ 1188327-79-8 ]
  • 3
  • [ 61-31-4 ]
  • [ 5121-00-6 ]
YieldReaction ConditionsOperation in experiment
95.6% The 250 ml flask is added in three 20.8g (0.1mol) naphthalene sodium acetate, adding proper amount of water, heated to make it dissolve, to take advantage of heat in concentrated hydrochloric acid (36%) acidified, adjusting pH to 2-3, cooling, filtering, results in the naphthalene acetic acid a white solid, drying, the white solid obtained 18.2g, yield 97.8%.To 50 ml by adding three-port flask are sequentially added 18.6g (0.1mol) naphthalene acetic acid, 150 ml toluene, 14.3g (0.12mol) thionyl chloride, stirring the mixture at room temperature for next adds by drops 0.2mLN, N-dimethyl formamide, heating reflow 2h. TLC monitoring the completion of reaction, the spin vaporization of the solvent and the excess of thionyl chloride, to obtain 19.6g pale yellow oily liquid, yield of 95.6%.
  • 4
  • [ 5121-00-6 ]
  • [ 57322-44-8 ]
  • 4-methyl-1-naphthylmethyl 1-naphthylacetate [ No CAS ]
 

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