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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225074Generated: October 30, 2026

Tributylstannane → 1-Tri-n-butylstannyl-4-p-fluorophenoxy-3-trimethylsilyloxy-trans-1-butene

https://huagongshe.com/reaction/225074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
Reactant{[1-(4-Fluorophenoxy)but-3-yn-2-yl]oxy}(trimethyl)silaneHCID 12786217—
CatalystAzobisisobutyronitrileHCID 6547—
Product1-Tri-n-butylstannyl-4-p-fluorophenoxy-3-trimethylsilyloxy-trans-1-buteneHCID 1278621885%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 2.52 g (10 mmoles) of 3-trimethylsilyloxy-4-p-fluorophenoxy-1-butyne (Example 158), 2.91 g (10 mmoles) of tri-n-butyl-tin hydride, and 10 mg of azobisiso-butyronitrile is heated, under an argon atmosphere, with stirring, for 2 hours at 140° C. After cooling to room temperature, the crude reaction mixture is fractionally distilled at 180°-185° C. (0.05 mm), to give 4.6 g (85%) of the subject product as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235797
Source datasetuspto-grants-1980_11
ORD IDord-c4586813347e41689122e53c461abb82
Source noteuspto-grants-1980_11