HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178591Generated: October 29, 2026
Benzyl chloroformate → Benzyl 3-(1,3,4-oxadiazol-2-yl)phenylcarbamate
https://huagongshe.com/reaction/2178591
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(1,3,4-Oxadiazol-2-yl)aniline | HCID 16228097 | — |
| Reactant | Propan-2-one--water (1/1) | HCID 18366337 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl 3-(1,3,4-oxadiazol-2-yl)phenylcarbamate | HCID 66851996 | 93% |
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 flit 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067933B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-8788ed8f93c94fc4ab5754a91e32b420 |
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| Source note | uspto-grants-2015_06 |
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