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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356042Generated: November 2, 2026

Diisopropylamine → Methyl n-(tert-butoxycarbonyl)-s-phenylcysteinate

https://huagongshe.com/reaction/2356042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantThiophenolHCID 7969—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN-Boc-L-serine methyl esterHCID 7019177—
SolventDichloromethaneHCID 6344—
ProductMethyl n-(tert-butoxycarbonyl)-s-phenylcysteinateHCID 18637399—

Reaction Steps

A 0° C. solution of N-(tert-butoxycarbonyl)-L-serine methyl ester (30 g, 137 mmol) and diisopropylamine (58 mL, 330 mmol) in dichloromethane (250 mL) was treated with methanesulfonyl chloride (11.65 mL, 151 mmol), stirred for 20 minutes, treated with thiophenol (15.5 mL, 151 mmol), warmed to room temperature, stirred for 30 minutes, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 10% ethyl acetate/hexanes to provide the desired product. MS (ESI(−)) m/e 310 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754886B2
Source datasetuspto-grants-2010_07
ORD IDord-a5ff2804f5fd4a29ae4e9cce05951abb
Source noteuspto-grants-2010_07