HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018109Generated: November 2, 2026
Methyl 4-ethynylbenzoate → HCID 9863994, compound
https://huagongshe.com/reaction/1018109
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-ethynylbenzoate | HCID 640163 | — |
| Reactant | HCID 18406081 | HCID 18406081 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Piperidine | HCID 8082 | — |
| Product | HCID 9863994 | HCID 9863994 | 46.3% |
Reaction Steps
To 478 mg (1.59 mmol) of 8-bromo-5-methoxymethyl-5-methyl-2,3,4,5-tetrahydrobenzo[b]thiepine, dissolved in 2.9 ml of piperidine, was added successively 4.8 mg (0.02 eq.) of CuI, 7.0 mg (0.02 eq.) of Ph3P, and 24.1 mg (0.01 eq.) of (Ph3P)4Pd. After heating to 80° C., a solution of 508 mg (2 eq.) of 4-ethynyl-benzoic acid methyl ester in 2.8 ml of piperidine was added within 2 h via dropping funnel and then kept at this temperature for 3 additional h. After cooling, the reaction mixture was poured onto crushed ice/ HCl diluted, extracted with diethylether, the organic phase was washed with water, dried over magnesium sulfate, filtrated and evaporated to dryness. Flash chromatography (SiO2, hexane/ethylacetate 95/5) yielded 270 mg of the title compound as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479670B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-ab8bde07afa641e7973188a8bd98d2e4 |
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| Source note | uspto-grants-2002_11 |
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