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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362305Generated: November 3, 2026

(3-Chloro-7-fluoro-benzo[b]thiophen-2-yl)methanol → 3-Chloro-7-fluoro-benzo[b]thiophene-2-carbaldehyde

https://huagongshe.com/reaction/1362305

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Chloro-7-fluoro-benzo[b]thiophen-2-yl)methanolHCID 59277539—
CatalystManganese dioxideHCID 14801—
SolventBenzeneHCID 241—
Product3-Chloro-7-fluoro-benzo[b]thiophene-2-carbaldehydeHCID 59277554102.2%

Reaction Steps

A suspension of (3-chloro-7-fluoro-benzo[b]thiophen-2-yl)methanol (600 g, 2.78 mmol) and MnO2 (1.69 g, 19.5 mmol) in benzene (25 mL) was stirred at room temperature for 2 d. The solution was filtered through diatomaceous earth and the filtrate concentrated to give the title compound (610 mg, quantitative) as a light, yellow solid: 1H NMR (300 MHz, CDCl3) δ 10.35 (s, 1H), 7.83 (d, J=8.1 Hz, 1H), 7.51 (ddd, J=8.0, 8.0, 4.8 Hz, 1H), 7.32-7.26 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-123ffa9e27be41f4b8e21e68899e3ec7
Source noteuspto-grants-2011_02