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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115203Generated: October 30, 2026

Di(3-thienyl)methanol → Di(3-thienyl)methanone

https://huagongshe.com/reaction/2115203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi(3-thienyl)methanolHCID 288490—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductDi(3-thienyl)methanoneHCID 573773—

Reaction Steps

To 2.1 gm (10.7 mmol) of Di-thiophen-3-yl-methanol in 50 mL of dichloromethane at room temperature was added 3.0 gm (13.9 mmol) of PCC. The reaction suspension was allowed to stir 2 hrs at room temperature. After 2 hrs, the reaction mixture was filtered and precipitates were washed with dichloromethane. The combined filtrates were concentrated. The concentrated sample was purified by flashy chromatography (hexane:ethyl acetate, from 11 to 18% ethyl acetate over 16 column volume) to obtain 1.83 gm (88.0%) of light yellow crystals; 1H NMR 500 MHz (CDCl3) δ 8.02 (d, 1H), 8.01 (d, 1H), 7.62 (d, 1H), 7.61 (d, 1H), 7.40 (d, 1H), 7.38 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435822B2
Source datasetuspto-grants-2008_10
ORD IDord-75425183eb354c81a770cf9fa6f8368a
Source noteuspto-grants-2008_10