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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232513Generated: October 26, 2026

Pivaloyl chloride → HCID 23358677, compound

https://huagongshe.com/reaction/232513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 178470518HCID 178470518—
SolventTolueneHCID 1140—
ProductHCID 23358677HCID 2335867759%

Reaction Steps

A solution of ethyl tetrazole-5-carboxylate (8.53 g, 60 mmol) and pivaloyl chloride (7.23 g, 60 mmol) in dry toluene (240 ml) is refluxed for 16 hours. After the solution has cooled to room temperature, it is washed two times with 1 N sodium hydroxide solution (20 ml) and then once with water (20 ml). The organic phase is dried over magnesium sulphate and the solvent is evaporated in vacuo to give ethyl 5-tert-butyl-[1,3,4]oxadiazole-2-carboxylate as a red oil (6.96 g, 59%), which is used in the following stage without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591695
Source datasetuspto-grants-1997_01
ORD IDord-e23c033927d345e494a2d38ec380f669
Source noteuspto-grants-1997_01