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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240815Generated: November 5, 2026

Phenyltrimethylammonium bromide dibromide → 2-Bromo-1-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-ethanone

https://huagongshe.com/reaction/2240815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
ReactantHCID 57508884HCID 57508884—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-1-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-ethanoneHCID 5750890780%

Reaction Steps

To a solution of 1-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-ethanone (1.18 g, 5.31 mmol, Example C) in THF (60 mL) and methanol (6 mL), phenyltrimethylammonium bromide dibromide (2.0 g, 5.31 mmol) is added in portions. Upon complete addition, the mixture is stirred at rt for 30 min before the solvent is evaporated. The crude product is purified by prep. HPLC (Grom-Sil 120 ODS-4-HE, 30×75 mm, 10 μm, 20-95% acetonitrile in water containing 0.5% formic acid) to give 2-bromo-1-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-ethanone (1.28 g) as a colourless oil; 1H NMR (CDCl3): δ 4.24 (s, 2H), 3.03 (t, J=7.0 Hz, 2H), 2.36 (s, 3H), 2.30 (s, 2H), 1.54 (t, J=7.0 Hz, 2H), 0.98 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723378B2
Source datasetuspto-grants-2010_05
ORD IDord-41709029bdde4892978f9ef2c467dc7d
Source noteuspto-grants-2010_05