Ethanethiol → Ethyl 2-[[4-hydroxybenzenesulfonyl](isobutyl)amino]acetate

HRID 742055Notes

Reaction equation

HRID 742055 reaction equation
C(S)C.[Al].C[O:6][C:7]1[CH:12]=[CH:11][C:10]([S:13]([N:16]([CH2:23][CH:24]([CH3:26])[CH3:25])[CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])(=[O:15])=[O:14])=[CH:9][CH:8]=1>C(Cl)Cl>[OH:6][C:7]1[CH:12]=[CH:11][C:10]([S:13]([N:16]([CH2:23][CH:24]([CH3:25])[CH3:26])[CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])(=[O:15])=[O:14])=[CH:9][CH:8]=1

Participants

5

Reactant 3

HCID 6343EthanethiolHCID 5359268AluminumHCID 10640094Ethyl 2-[[4-methoxybenzenesulfonyl](isobutyl)amino]acetate

Product 1

HCID 10591435Ethyl 2-[[4-hydroxybenzenesulfonyl](isobutyl)amino]acetate

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

A solution of ethanethiol (15 mL) and methylene chloride (15 mL) is cooled to 0° C. Aluminum trichlofide (9.62 g, 72.2 mmol) is added (the solution turns green), and the reaction is warmed to room temperature. Ethyl 2-[[4-methoxybenzenesulfonyl](isobutyl)-amino]acetate (4.75 g, 14.44 mmol) is added in methylene chloride (5 mL), and the reaction is stirred for 3.5 hours at room temperature. The reaction is then slowly quenched with water, and the crude reaction is partitioned between water and methylene chloride. The aqueous layer is extracted well with methylene chloride, the combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (25% to 50% ethyl acetate/hexane) to give ethyl 2-[[4-hydroxybenzenesulfonyl](isobutyl)amino]acetate.

Workup

  1. customThe reaction is then slowly quenched with water
  2. customthe crude reaction
  3. customis partitioned between water and methylene chloride
  4. extractionThe aqueous layer is extracted well with methylene chloride
  5. dry with materialthe combined organic layers are dried (Na2SO4)
  6. customthe solvent is evaporated
  7. customThe product is purified by silica gel chromatography (25% to 50% ethyl acetate/hexane)

Sources & evidence

ORD record
ord-9afe8ac81c8e40299b0c193456aa3049
Source dataset
uspto-grants-1996_09
Patent number
US05552419

Reaction notes

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