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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852555Generated: October 30, 2026

Triethylamine → 3-(4-Chloro-butanoylamino)-5-methylsulfanyl-benzoic acid methyl ester

https://huagongshe.com/reaction/852555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chlorobutyryl chlorideHCID 78370—
Reactant3-Amino-5-methylsulfanyl-benzoic acid methyl ester hydrochlorideHCID 69357596—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-(4-Chloro-butanoylamino)-5-methylsulfanyl-benzoic acid methyl esterHCID 69357700103.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-amino-5-methylsulfanyl-benzoic acid methyl ester hydrochloride (D62) (0.13 g, 0.556 mmol, 1 equiv) in dry CH2Cl2 (2 ml) at 0° C. was added NEt3 (193 ml, 1.39 mmol, 2.5 equiv) then 4-chlorobutyryl chloride (69 ml, 0.612 mmol, 1.1 equiv), dropwise, over 2 min. The resulting solution was stirred at 0° C. for 15 min then at room temperature for 30 min. The solution was then diluted with AcOEt, washed sequentially with 2N aqueous HCl solution, saturated aqueous NaHCO3 solution and brine, dried over Na2SO4 and concentrated in vacuo to give 3-(4-chloro-butanoylamino)-5-methylsulfanyl-benzoic acid methyl ester (D64) (173 mg, 103%) as pale yellow crystals. [M+H]+=302.0, RT=3.20 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-6ed46d440efe4513ae9c5a11f1d3fda9
Source noteuspto-grants-2007_08