Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719294Generated: November 1, 2026

Tributylstannane → HCID 70518003, compound

https://huagongshe.com/reaction/1719294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantHCID 86738872HCID 86738872—
SolventBenzeneHCID 241—
ProductHCID 70518003HCID 7051800378.8%

Reaction Steps

A mixture of methyl 4-[(2R,3R)-3-isocyano-4-oxoazetidin-2-yl]-3-methoxybut-2-enoate[(E,Z)-isomeric mixture](50 mg), tri-n-butyltin hydride (90 μl), and 2,2'-azobis-(2-methylpropionitrile) (5 mg) in benzene (5 ml) was heated to reflux for one hour under a nitrogen atmosphere. The reaction mixture was cooled to room temperature and chromatographed on silica gel (2.5 g) eluting first with dichloromethane and then 4% methanol in dichloromethane to give methyl 3-methoxy-4-[(2R)-4-oxoazetidin-2-yl]but-2-enoate[(E,Z)-isomeric mixture](35 mg) as a crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539152
Source datasetuspto-grants-1985_09
ORD IDord-3cf0d9f186e041cea8895319f797d399
Source noteuspto-grants-1985_09