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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071061Generated: November 1, 2026

Carbon tetrabromide → tert-Butyl [(5-methyl-1,3,4-oxadiazol-2-yl)methyl]carbamate

https://huagongshe.com/reaction/2071061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantAcetohydrazideHCID 14039—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantCarbonylimidazoleHCID 13571086—
SolventDichloromethaneHCID 6344—
Producttert-Butyl [(5-methyl-1,3,4-oxadiazol-2-yl)methyl]carbamateHCID 57366760107.9%

Reaction Steps

To a stirred solution of Boc-Glycine (1.75 g, 10.0 mmol) in CH2Cl2 at 0° C. was added carbonyl imidazole (1.7 g, 10.5 mmol) and the reaction was stirred for 30 min and then acetic hydrazide (740 mg, 10.0 mmol) was added. After 45 min, CBr4 (6.63 g, 20.0 mmol) and PPh3 (5.25 g, 20.0 mmol) were added and the reaction was stirred overnight at room temperature. The reaction mixture was concentrated partially and chromatographed (50% EtOAc in hexanes) to provide 2.3 g of tert-butyl (5-methyl-1,3,4-oxadiazol-2-yl)methylcarbamate with some triphenylphosphine oxide as impurity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-d0362ba986db4ab38717d9d120190627
Source noteuspto-grants-2012_10