HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395166Generated: October 29, 2026
Tributylstannane → 1-Tri-n-butylstannyl-4-p-fluorophenoxy-3-trimethylsilyloxy-trans-1-butene
https://huagongshe.com/reaction/1395166
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | {[1-(4-Fluorophenoxy)but-3-yn-2-yl]oxy}(trimethyl)silane | HCID 12786217 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Product | 1-Tri-n-butylstannyl-4-p-fluorophenoxy-3-trimethylsilyloxy-trans-1-butene | HCID 12786218 | 85% |
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 azobisisobutyronitrile 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04202822 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-079664dc05664947a68ef7bfa8b008d4 |
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| Source note | uspto-grants-1980_05 |
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