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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921671Generated: October 30, 2026

Tert-butyl 4-(1-allyloxycarbonylaminocyclopropyl)benzoate → 4-(1-{[(Prop-2-en-1-yloxy)carbonyl]amino}cyclopropyl)benzoic acid

https://huagongshe.com/reaction/1921671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(1-allyloxycarbonylaminocyclopropyl)benzoateHCID 59305799—
SolventAcetonitrileHCID 6342—
Product4-(1-{[(Prop-2-en-1-yloxy)carbonyl]amino}cyclopropyl)benzoic acidHCID 59305810—

Reaction Steps

A solution of 1.46 g of tert-butyl 4-(1-allyloxycarbonylaminocyclopropyl)benzoate in 10 mL of acetonitrile was combined with 1 g of montmorillonite and refluxed for 3 hours. Then more montmorillonite was added and the mixture was boiled for 4 hours. The suspension was filtered hot, the inorganic material was extracted 3× with hot acetonitrile and filtered off, and the acetonitrile solutions were combined and evaporated down. Residue: 0.8 g of crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173699B2
Source datasetuspto-grants-2012_05
ORD IDord-544d58a635b94750a559f41d56150187
Source noteuspto-grants-2012_05