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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389613Generated: October 30, 2026

Benzyl chloroformate → Benzyl 3-(1,3,4-oxadiazol-2-yl)phenylcarbamate

https://huagongshe.com/reaction/389613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(1,3,4-Oxadiazol-2-yl)anilineHCID 16228097—
ReactantPropan-2-one--water (1/1)HCID 18366337—
SolventWaterHCID 962—
ProductBenzyl 3-(1,3,4-oxadiazol-2-yl)phenylcarbamateHCID 6685199693%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-(1,3,4-oxadiazol-2-yl)aniline (1 g, 6.2 mmol) and sodium bicarbonate (1.1 g, 13 mmol) in a 2:1 mixture of acetone/water (10 mL) was cooled to 0° C. Benzylchloroformate (0.92 mL, 6.5 mmol) was added dropwise over 5 minutes. The reaction mixture was brought to room temperature and stirred for 30 minutes at which point LCMS indicated completion of the reaction. The reaction mixture was diluted with water and filtered on a glass frit to give (3-[1,3,4]Oxadiazol-2-yl-phenyl)-carbamic acid benzyl ester as a white powder (1.7 g, 93%). M+1=296.4

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378108B2
Source datasetuspto-grants-2013_02
ORD IDord-2e2d410a7fe643c2b535f3833976a962
Source noteuspto-grants-2013_02