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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742378Generated: November 1, 2026

Ethanol → HCID 15232314, compound

https://huagongshe.com/reaction/1742378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
ReactantHCID 15337559HCID 15337559—
ReactantHCID 131718643HCID 131718643—
ProductHCID 15232314HCID 1523231423%

Reaction Steps

A mixture of 3-phenylmethylene-8-azabicyclo[3.2.1]octane (1.09 g, 4.87 mmol), 4-(triisopropylsiloxy-alpha-bromopropiophenone (1.88 g, 4.88 mmol) and triethylamine (1.5 ml, 10.76 mmol) in ethanol (75 ml) was refluxed 22 hours. After cooling, ether (50 ml) was added and the mixture was filtered through diatomaceous earth. The filtrate was concentrated and chromatographed on silica gel (2×6 inches, hexane then ethyl acetate/hexane gradient) to give 0.56 g (23%) of an orange oil product; NMR 8.18 (d, 2H), 7.25 (t, 2H), 7.12 (d, 3H), 6.86 (d, 2H), 6.29 (s, 1H), 4.08 (m, 1H), 3.47-3.26 (m, 2H), 2.75 (m, 1H), 2.57-2.37 (m, 2H), 2.03-1.72 (m, 4H), 1.6 (m, 1H; partially under water peak from NMR solvent), 1.40 (d, 3H), 1.25 (m, 3H), 1.09 (d, 18H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338754
Source datasetuspto-grants-1994_08
ORD IDord-71721a35c77f48e6b3bd6d3dc3d70264
Source noteuspto-grants-1994_08