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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714142Generated: October 29, 2026

Hexachloroethane → METHYL N-BOC-3-CHLORO-L-ALANINATE

https://huagongshe.com/reaction/714142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexachloroethaneHCID 6214—
ReactantTriphenylphosphineHCID 11776—
ReactantN-Boc-L-serine methyl esterHCID 7019177—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
SolventHCID 87695156HCID 87695156—
ProductMETHYL N-BOC-3-CHLORO-L-ALANINATEHCID 1218279461.4%

Reaction Steps

A solution of triphenylphosphine (4.55 g, 17.4 mmol) and hexachloroethane (3.9 g, 16.5 mmol) in 1,2-dichloroethane (18 mL) prepared at 0° C. was added via cannula into a flask containing a solution of methyl N-(tert-butoxycarbonyl)-L-serinate (3.2 g, 14.6 mmol) in 1,2-dichloroethane DCE (40 mL), kept at 0° C. under N2 atmosphere. After the addition was completed, the reaction mixture was further stirred at room temperature for 2 h, diluted with DCM, washed with sat NaHCO3, dried over MgSO4, filtered and concentrated. Purification made through chromatographic column of silicagel eluted with 10% to 50% EtOAc in hexane for 30 min, to afford 2.13 g (61% yield) of title compound as white crystals. MS: m/z=260.0 (MNa+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187415B2
Source datasetuspto-grants-2015_11
ORD IDord-632dce4151594184ab5a458779f8e933
Source noteuspto-grants-2015_11