HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pivaloyl chloride → HCID 23358677, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | HCID 178470518 | HCID 178470518 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 23358677 | HCID 23358677 | 59% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05591695 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-e23c033927d345e494a2d38ec380f669 |
| Source note | uspto-grants-1997_01 |