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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018109Generated: November 2, 2026

Methyl 4-ethynylbenzoate → HCID 9863994, compound

https://huagongshe.com/reaction/1018109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-ethynylbenzoateHCID 640163—
ReactantHCID 18406081HCID 18406081—
CatalystTriphenylphosphineHCID 11776—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventPiperidineHCID 8082—
ProductHCID 9863994HCID 986399446.3%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479670B1
Source datasetuspto-grants-2002_11
ORD IDord-ab8bde07afa641e7973188a8bd98d2e4
Source noteuspto-grants-2002_11