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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894618Generated: October 30, 2026

Benzyl chloroformate → 5-benzyloxycarbonylaminospiro[benzo[b]furan-2(3H), 1'-cyclopropane]-3-one

https://huagongshe.com/reaction/894618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantHCID 12925991HCID 12925991—
SolventPyridineHCID 1049—
Product5-benzyloxycarbonylaminospiro[benzo[b]furan-2(3H), 1'-cyclopropane]-3-oneHCID 12925998—

Reaction Steps

To a solution of 5-aminospiro[benzo[b]furan-2(3H), 1'-cyclopropane]-3-one (1.35 g.) in pyridine (13.5 ml.) was added carbobenzyloxy chloride (30% toluene solution, 7 g.) under ice-cooling, and the mixture stirred for one hour. The reaction mixture was poured into ice-hydrochloric acid (14 ml.) and extracted with ethyl acetate. The extract was washed with water, dried and concentrated to remove the solvent. The residue was recrystallized from ethanol. By the above procedure there was obtained 5-benzyloxycarbonylaminospiro[benzo[b]furan-2(3H), 1'-cyclopropane]-3-one as pale yellow needles, m.p. 118°-119° C. Yield 1.57 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284644
Source datasetuspto-grants-1981_08
ORD IDord-cd7e0b0436c54ed685bc6dfcccb3b37d
Source noteuspto-grants-1981_08