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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572065Generated: October 31, 2026

Triethylamine → (5-tert-Butyl-[1,3,4]oxadiazol-2-yl)-carbamic acid 2,2,2-trichloro-ethyl ester

https://huagongshe.com/reaction/572065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
Reactant5-tert-Butyl-1,3,4-oxadiazol-2-amineHCID 13381393—
SolventAcetonitrileHCID 6342—
Product(5-tert-Butyl-[1,3,4]oxadiazol-2-yl)-carbamic acid 2,2,2-trichloro-ethyl esterHCID 8668668473.3%

Reaction Steps

To a suspension of 5-tert-butyl-[1,3,4]oxadiazol-2-ylamine (Atlantic, 141 mg, 1.00 mmol) and Et3N (279 μL, 2.00 mmol) in MeCN (2 mL), 2,2,2-trichloroethyl chloroformate (207 μL, 1.50 mmol) was added in 4 portions over 1 min at RT (CARE: exotherm to −40° C.). The resulting suspension was stirred for 1 h. The suspension was filtered, washing the solid with MeCN (3 mL), and concentrated to leave a yellow-brown paste. Purification by FCC, using 0-2.5% MeOH in DCM, gave a buff foam (232 mg, 73%). 1H NMR (400 MHz, CDCl3): 1.42 (9H, s), 4.86 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029373B2
Source datasetuspto-grants-2015_05
ORD IDord-07af86e407f94599aa7af270603976fb
Source noteuspto-grants-2015_05