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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701671Generated: October 31, 2026

Tributylstannane → HCID 53866326, compound

https://huagongshe.com/reaction/1701671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantBenzhydryl 2-(3-phenoxyacetamido-4-chloro-2oxoazetidin-1-yl)-3-methyl-2-butenoateHCID 20534636—
ReactantHCID 86736893HCID 86736893—
SolventTolueneHCID 1140—
ProductHCID 53866326HCID 53866326—

Reaction Steps

Benzhydryl 2-(3-phenoxyacetamido-4-chloro-2-oxoazetidin-1-yl)-3-methyl-4-methoxy-2-butenoate [prepared from benzhydryl 2-(3-phenoxyacetamido-4-chloro-2oxoazetidin-1-yl)-3-methyl-2-butenoate using the general procedures described in Examples 7 and 8(A) hereinabove] (264 mg, 0.5 mmol) was dissolved in 1 ml of toluene with 0.6 mmol of tri(butyl)tin hydride and 0.6 mmol of azobisisobutyronitrile (99 mg) and heated at 62° with stirring under a nitrogen atmosphere. The reaction solvent was removed under reduced pressure to provide an impure product which was purified by preparative thin layer chromatography. (1:2/ethyl acetate:hexane). Yield --54 mg of title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04195021
Source datasetuspto-grants-1980_03
ORD IDord-ecade2371fa243ceb1578f345bf8059b
Source noteuspto-grants-1980_03