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Chemical Structure| 120042-11-7 Chemical Structure| 120042-11-7

Structure of Boc-Hse-OMe
CAS No.: 120042-11-7

Chemical Structure| 120042-11-7

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Product Details of [ 120042-11-7 ]

CAS No. :120042-11-7
Formula : C10H19NO5
M.W : 233.26
SMILES Code : O=C(OC)[C@@H](NC(OC(C)(C)C)=O)CCO
MDL No. :MFCD09835542
InChI Key :IWNVPOPPBRMFNG-ZETCQYMHSA-N
Pubchem ID :10561607

Safety of [ 120042-11-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 120042-11-7 ]

* 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 [ 120042-11-7 ]

[ 120042-11-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 120042-11-7 ]
  • [ 76969-87-4 ]
YieldReaction ConditionsOperation in experiment
78% With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 20℃; for 16h; 3. (L) -2-tert-Butoxycarbonylamino-4-bromobutyric acid methyl ester; A solution of (L) -N-tert-butoxycarbonylhomoserine methyl ester (1.2 g, 5.14 mmol) and carbontetrabromide (2.52 g, 7.71 mitiol) in dichloromethane (20 mL) was treated with a second solution of triphenylphosphine (1.34 g, 5.14 mmol) in dichloromethane (15 mL) . After stirring at room temperature for 16 h, the solution was diluted with heptane (50 mL) . The resulting precipitate was filtered and successively washed with heptane, 5% NaHCO3, sat. aq NaCl, dried over MgSO4 and concentrated. Purification by by flash column chromatography (10% ethyl acetate in heptane) gave (L) -2-tert- butoxycarbonylamino-4-bromobutyric acid methyl ester as white solid (1.19 g, 78%) .
78% With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 20℃; for 16h; To a mixture of (S)-methyl 2-(tert-butoxycarbonylamino)-4-hydroxybutanoate (0.6 g, 2.57 mmol) and carbon tetrabromide (1.26 g, 3.9 mmol) in DCM (10 mL) was added a solution of triphenylphosphine (0.67 g, 2.6 mmol) in DCM (8 mL). The mixture was stirred at r.t. for 16 hr then triturated with heptane (25 mL) and filtered. The filtrate was successively washed with heptane, aqueous NaHCC (5%wt) and brine. The organic was separated, dried over anhydrous MgSC , and concentrated under reduced pressure. The residue was purified by flash column chromatography to afford the desired product (0.6 g, 78% yield) as white solid. LC-MS: m/z: 296 (M+H)+.
78% With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 20℃; for 16h; A solution of (L) -N-tert-butoxycarbonylhomoserine methyl ester (1.2 g, 5.14 mmol) and carbontetrabromide (2.52 g, 7.71 mmol) in dichloromethane (20 mL) was treated with a second solution of triphenylphosphine (1.34 g, 5.14 mmol) in dichloromethane (15 mL). After stirring at room temperature for 16 h, the solution was diluted with heptane (50 mL). The resulting precipitate was filtered and successively washed with heptane, 5% NAHCO3, sat. aq NaCl, dried over MGS04 AND concentrated. Purification by by flash column chromatography (10% ethyl acetate in heptane) gave (L)-2-tert- butoxycarbonylamino-4-bromobutyric acid methyl ester as white solid (1.19 g, 78%). 1H NMR (CDC13), 8 5-10 (D, LT = 5 Hz, 1 H), 4. 38 (t, J = 15 Hz, 1 H), 3.77 (s, 3 H), 3.44 (t, J = 13 Hz, 2 H), 2.40 (m, 1 H), 2.21 (M, 1 H), 1.42 (s, 9 H).
  • 2
  • [ 98045-03-5 ]
  • [ 120042-11-7 ]
  • 3
  • CBr4 [ No CAS ]
  • [ 120042-11-7 ]
  • [ 76969-87-4 ]
YieldReaction ConditionsOperation in experiment
76% With triphenylphosphine; In dichloromethane; Step D: (S)4-Bromo-2-tert-butoxycarbonylaminobutyric acid methyl ester To a cooled (0 C.) solution of (S)-2-tert-butoxycarbonylamino-4-hydroxy-butyric acid methyl ester (28.7 g,123 mmol) in dichloromethane (500 mL) was added CBr4 (51.0 g, 154 mmol). The mixture was stirred for 5 minutes before the portion-wise addition of triphenylphosphine (48.41 g, 185 mmol). The mixture continued to stir at 0 C. for 1 hour and was then allowed to warm to room temperature. The solvent was removed under reduced pressure and was then diluted with ether (500 mL) and stirred for 30 minutes. The mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was chromatographed eluding with ether/hexanes (1:2) to afford 27.5 g of white solid (76% yield).
 

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