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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240635Generated: November 1, 2026

Allyl chloroformate → Tert-butyl 4-(1-allyloxycarbonylaminocyclopropyl)benzoate

https://huagongshe.com/reaction/2240635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chloroformateHCID 18052—
ReactantTert-butyl 4-(1-aminocyclopropyl)benzoateHCID 59305811—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(1-allyloxycarbonylaminocyclopropyl)benzoateHCID 59305799—

Reaction Conditions

Temperature0 °C

Reaction Steps

3 g of tert-butyl 4-(1-aminocyclopropyl)benzoate was placed in 30 mL of dichloromethane and 1.8 mL of pyridine. The solution was cooled to 0° C. and 1.2 mL of allyl chloroformate (dissolved in 5 mL of dichloromethane) was added dropwise at 0° C.-5° C. The mixture was left to react for 30 minutes at 0° C. and 2 hours at RT. The solution was combined with silica gel and evaporated down to the residue. This was chromatographed with dichloromethane on silica gel 70. Yield: 1.46 g of oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723381B2
Source datasetuspto-grants-2010_05
ORD IDord-6694c2a70f8044e589df03ded05a9648
Source noteuspto-grants-2010_05