4-Methoxybenzenesulfonyl chloride → N-(4-methoxybenzenesulfonyl)-D-valine benzyl ester

HRID 1604299Notes

Reaction equation

HRID 1604299 reaction equation
Cl.[CH2:2]([O:9][C:10](=[O:16])[C@@H:11]([CH:13]([CH3:15])[CH3:14])[NH2:12])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C(N(CC)CC)C.[CH3:24][O:25][C:26]1[CH:31]=[CH:30][C:29]([S:32](Cl)(=[O:34])=[O:33])=[CH:28][CH:27]=1>O.O1CCOCC1>[CH2:2]([O:9][C:10](=[O:16])[C@@H:11]([CH:13]([CH3:14])[CH3:15])[NH:12][S:32]([C:29]1[CH:28]=[CH:27][C:26]([O:25][CH3:24])=[CH:31][CH:30]=1)(=[O:34])=[O:33])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

Participants

6

Reactant 3

HCID 74014-Methoxybenzenesulfonyl chlorideHCID 8471TriethylamineHCID 56777379D-valine benzyl ester hydrochloride

Product 1

HCID 15429254N-(4-methoxybenzenesulfonyl)-D-valine benzyl ester

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 312751,4-DioxaneSolvent

Procedure

To a solution of D-valine benzyl ester hydrochloride (2.4 grams, 10 mmol) and triethylamine (2.5 grams, 3.5 mL, 25 mmol) in water (50 mL) and 1,4-dioxane (50 mL) is added 4-methoxybenzenesulfonyl chloride (2.3 grams, 11 mmol). The mixture was stirred at room temperature for 1 hour and then most of the solvent was removed by evaporation under vacuum. The mixture was diluted with ethyl acetate and was washed successively with dilute hydrochloric acid solution, water and brine. The organic solution was dried over magnesium sulfate and concentrated to leave N-(4-methoxybenzenesulfonyl)-D-valine benzyl ester as a while solid, 3.6 grams (97%); m.p. 92-94° C.

Workup

  1. custommost of the solvent was removed by evaporation under vacuum
  2. additionThe mixture was diluted with ethyl acetate
  3. washwas washed successively with dilute hydrochloric acid solution, water and brine
  4. dry with materialThe organic solution was dried over magnesium sulfate
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-b2fb366e7b0e443a99e04ac857785e9d
Source dataset
uspto-grants-1999_11
Patent number
US05994351

Reaction notes

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