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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053706Generated: October 31, 2026

Bis(2-chloroethyl)carbamoyl chloride → tert-Butyl 3-[5-[bis(2-chloroethyl)carbamoyloxy]-2-methyl-phenyl]-4-(tert-butoxycarbonylamino)butanoate

https://huagongshe.com/reaction/1053706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(2-chloroethyl)carbamoyl chlorideHCID 76346—
Reactanttert-Butyl 4-(tert-butoxycarbonylamino)-3-(5-hydroxy-2-methyl-phenyl)butanoateHCID 118277046—
SolventPyridineHCID 1049—
Producttert-Butyl 3-[5-[bis(2-chloroethyl)carbamoyloxy]-2-methyl-phenyl]-4-(tert-butoxycarbonylamino)butanoateHCID 118276980—

Reaction Steps

Adapting a literature known protocol (U.S. Pat. No. 3,299,104), tert-butyl 3-[5-[bis(2-chloroethyl)carbamoyloxy]-2-methyl-phenyl]-4-(tert-butoxycarbonylamino)butanoate (23e) is prepared through carbamoylation of tert-butyl 4-(tert-butoxycarbonylamino)-3-(5-hydroxy-2-methyl-phenyl)butanoate (23d) (731 mg, 2.0 mmol) with commercial N,N-bis(2-chloroethyl)carbamoyl chloride (439 μL, 614 mg, 3.0 mmol) in anhydrous pyridine (15 mL) at about 0° C. The reaction mixture is stirred with gradual warming to room temperature. The reaction is monitored by TLC and/or LC/MS to completion. Excess of the carbamoyl chloride is destroyed with crushed ice. Aqueous work-up followed by purification through silica gel column chromatography afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394236B2
Source datasetuspto-grants-2016_07
ORD IDord-a24794b1426c42008815ef84bc34cf67
Source noteuspto-grants-2016_07