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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909455Generated: October 30, 2026

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

https://huagongshe.com/reaction/1909455

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 numberUS08598360B2
Source datasetuspto-grants-2013_12
ORD IDord-ec70acd30ba04d0e885cbc006af69858
Source noteuspto-grants-2013_12