HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254475Generated: November 1, 2026
Stannane, tributyl-3-thienyl- → HCID 19744835, compound
https://huagongshe.com/reaction/2254475
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannane, tributyl-3-thienyl- | HCID 10959689 | — |
| Reactant | HCID 19744768 | HCID 19744768 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 19744835 | HCID 19744835 | 77% |
Reaction Steps
1.4 g of 3-bromomethylbenzaldehyde was dissolved in 3 ml of dimethylformamide, and the solution was added to 5 ml of a tetrahydrofuran solution of phenolate, prepared from 1.5 g of 3-bromophenol and 0.36 g of 60% oily sodium hydride. The mixture was stirred for 2 hours at room temperature. The solvent was evaporated, and water and ethyl acetate were added to the residue to extract it. The extract was worked up in a customary manner to give crude 3-(3-bromophenoxymethyl)benzaldehyde. When the same reaction as in Referential Example 12 was performed using 440 mg of the resulting aldehyde compound, 747 mg of tributyl(3-thienyl)stannane and 10 mg of tetrakis(triphenylphosphine)palladium, 341 mg (yield 77%) of 3-[3-(3-thienyl)phenoxymethyl)benzaldehyde was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05234946 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-c20ae219328f451abf0958ae9422edb1 |
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| Source note | uspto-grants-1993_08 |
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