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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251740Generated: November 2, 2026

Benzo(B)Thiophene → HCID 53641103, compound

https://huagongshe.com/reaction/1251740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantTetrahydrofuranHCID 8028—
ReactantVeratraldehydeHCID 8419—
ReactantHCID 178418306HCID 178418306—
ProductHCID 53641103HCID 53641103—

Reaction Steps

α-(2-benzo[b]thienyl)-3,4-dimethylbenzyl alcohol was prepared in the same manner as described in Example 40A. Reaction of benzo[b]-thiophene (7.5 mmoles, 1.0 g), t-BuLi (1.7 m, 97 mmoles, 5.7 ml) and 3,4-dimethoxybenzaldehyde (8.9 mmoles, 1.5 g) in THF (20 ml) yielded, after flash chromatography using 30% ethyl acetate/hexanes, 2.25 g (≈100%) of a white gummy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342610B2
Source datasetuspto-grants-2002_01
ORD IDord-c60769e6819146a8835dfccb379595f6
Source noteuspto-grants-2002_01