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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085710Generated: November 1, 2026

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

https://huagongshe.com/reaction/2085710

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 numberUS06720338B2
Source datasetuspto-grants-2004_04
ORD IDord-191ae1181d0140ba85e8cded5542844f
Source noteuspto-grants-2004_04