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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264573Generated: October 30, 2026

4-Methoxybenzenesulfonyl chloride → N-(4-Methoxybenzenesulfonyl)-L-serine, t-butyl ester

https://huagongshe.com/reaction/1264573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantTriethylamineHCID 8471—
Reactant(S)-tert-Butyl 2-amino-3-hydroxypropanoateHCID 11768865—
SolventDichloromethaneHCID 6344—
ProductN-(4-Methoxybenzenesulfonyl)-L-serine, t-butyl esterHCID 131721839101.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 12.18 g (0.0756 mol) of L-serine, t-butyl ester, 26.52 ml of triethylamine in 160 ml of CH2Cl2 (cooled in an ice bath) was added, in small portions, 16.1 g (0.0771 mol) of 4-methoxybenzene-sulfonyl chloride. The mixture was stirred at 0° C. for 0.5 hours and at room temperature overnight. The mixture was washed with H2O, 2N citric acid, brine and dried with Na2SO4. The solvent was removed under vacuum to give 25.34 g of solid which was triturated with hexane. The solid was recrystallized from 120 ml of toluene to give 12.18 g (48.7%) of product as a white solid. The filtrate was concentrated and the residue chromatographed on silica gel with hexane-ethyl acetate (7:3) as eluent to give 5.71 g (22.8%) of white solid. m.p. 70-75° C. Anal. for C14H21NO6S: Calc'd: C, 50.7; H, 6.4; N, 4.2; Found: C, 50.4; H, 6.3; N, 4.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544984B1
Source datasetuspto-grants-2003_04
ORD IDord-1f54d52e5bda4af695b36d8f83867475
Source noteuspto-grants-2003_04