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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097158Generated: October 31, 2026

1-Benzothiophen-5-ylmethanol → Benzo(b)thiophene-5-carboxaldehyde

https://huagongshe.com/reaction/2097158

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzothiophen-5-ylmethanolHCID 2795446—
CatalystManganese dioxideHCID 14801—
SolventBenzeneHCID 241—
ProductBenzo(b)thiophene-5-carboxaldehydeHCID 13909792.6%

Reaction Steps

Benzo[b]thiophen-5-ylmethanol (311 mg, 1.89 mmol) was dissolved in anhydrous benzene (20 mL). MnO2 (1317 mg, 15.2 mmol) was added and the reaction was stirred for 12 h. The solution was filtered through celite and the filter cake was washed with ethyl acetate (50 mL). The filtrate was concentrated under vacuum to give the product (284 mg, 92%) as an off-white solid: 1H NMR (400 MHz, DMSO-d6) δ 10.09 (s, 1H), 8.46-8.45 (m, 1H), 8.21 (d, J=8.4 Hz, 1H), 7.94 (d, J=5.6 Hz, 1H), 7.81 (dd, J=8.4, 1.2 Hz, 1H), 7.66 (d, J=5.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450307B2
Source datasetuspto-grants-2013_05
ORD IDord-5525e1371e8143b8a4987fd5db6a2e90
Source noteuspto-grants-2013_05