Water → [(4-Chlorobutyl)thio]acetic acid methyl ester

HRID 22962Notes

Reaction equation

HRID 22962 reaction equation
[C:1]([O:5][CH3:6])(=[O:4])[CH2:2][SH:3].C([Li])CCC.Br[CH2:13][CH2:14][CH2:15][CH2:16][Cl:17].O>O1CCCC1.C(OCC)(=O)C>[CH3:6][O:5][C:1](=[O:4])[CH2:2][S:3][CH2:13][CH2:14][CH2:15][CH2:16][Cl:17]

Participants

7

Procedure

A solution of methyl thioglycolate (10.0 mL, 113 mmol) in tetrahydrofuran (200 mL) at −78° C. under argon atmosphere was treated dropwise with n-butyllithium (2.5 M hexanes solution, 45 mL, 113 mmol). After 1 h at −78° C., the cloudy solution was rapidly treated with 1-bromo-4-chlorobutane (13.0 mL, 113 mmol) and allowed to warm to room temperature overnight. It was poured into water and hexanes, washed with cold aqueous sodium hydroxide solution (0.1 M) followed with saturated aqueous ammonium chloride, and the organic layer was stored over anhydrous sodium sulfate. The volatiles were removed and the residue was purified by chromatography and eluted with 8:1 hexane:ethyl acetate to yield [(4-chlorobutyl)thio]acetic acid methyl ester (10.7 g, 54.5 mmol) as a colorless liquid: EIMS m/z 198 (M+ with 37Cl), 196 (M+ with 35Cl).

Workup

  1. washwashed with cold aqueous sodium hydroxide solution (0.1 M)
  2. customThe volatiles were removed
  3. customthe residue was purified by chromatography
  4. washeluted with 8:1 hexane

Sources & evidence

ORD record
ord-bd2924b916214d3687817fa1319627de
Source dataset
uspto-grants-2005_02
Patent number
US06849657B2

Reaction notes

Loading…