Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482920Generated: October 30, 2026

tert-Butyl bromoacetate → HCID 131714543, compound

https://huagongshe.com/reaction/482920

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantPotassium cyanateHCID 11378442—
Reactanttert-Butyl ((2S,3S)-2-methyl-4-oxoazetidin-3-yl)carbamateHCID 13155285—
SolventDimethylformamideHCID 6228—
ProductHCID 131714543HCID 13171454320.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of potassium cyanate (186 mg, 2.3 mmol) in 2 ml of dimethylformamide was added t-butyl bromoacetate (0.356 ml, 2.2 mmol). The mixture was heated to 100° C. for 1 hour and cooled to room temperature. (3S-trans)-3-[[(t-Butyloxy)carbonyl]amino]-4-methyl-2-azetidinone (400 mg, 2.0 mmol) was then added, and the mixture was heated to 140° C. for 1 hour. Upon cooling to room temperature, the crude product was extracted from ice cold 5% HCl with three portions of ethyl acetate. The combined organic layers were extracted twice with water, once with aqueous potassium bicarbonate, and dried over sodium sulfate. The volatiles were removed, and the residue was subjected to chromatography on silica gel (eluting with 40% ethyl acetate-hexane) yielding 149 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04576749
Source datasetuspto-grants-1986_03
ORD IDord-cea0261d1bdc41cb871b20f45ec77301
Source noteuspto-grants-1986_03