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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452810Generated: October 31, 2026

Phenylacetylene → HCID 11119343, compound

https://huagongshe.com/reaction/1452810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
ReactantHCID 11130420HCID 11130420—
ProductHCID 11119343HCID 11119343—

Reaction Steps

The general procedure was used to convert phenylacetylene and (Z)-ethyl 3-iodo-3-phenylacrylate to the title product. Purification by flash chromatography (5% ethyl acetate in hexanes as the eluent) gave the analytically pure product as a light yellow oil (530 mg, 96% yield). 1H NMR (400 MHz, CDCl3) δ 7.78 (m, 2H), 7.63 (m, 2H), 7.38 (m, 6H), 6.59 (s, 1H), 2.06 (q, 2H), 1.35 (t, 3H). 13C NMR (100 MHz, CDCl3) δ 165.12, 136.92, 136.08, 131.85, 129.66, 128.99, 128.42, 128.18, 126.96, 122.54, 122.48, 101.88, 86.68, 60.16, 14.17. Anal. Calc'd. for C19H16O2: C, 82.58; H, 5.84; Found C,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473797B2
Source datasetuspto-grants-2009_01
ORD IDord-c71a3a3316004c0494cbfb120d3f1a79
Source noteuspto-grants-2009_01