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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738484Generated: October 30, 2026

Benzo(B)Thiophene → a-(2-Benzo[b]thienyl)-3,4-dimethoxybenzyl alcohol

https://huagongshe.com/reaction/1738484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantVeratraldehydeHCID 8419—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Producta-(2-Benzo[b]thienyl)-3,4-dimethoxybenzyl alcoholHCID 49962621—

Reaction Steps

α-(2-benzo[b]thienyl)-3,4-dimethoxybenzyl 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 aceteate/hexanes, 2.25 g (≈100%) of a white gummy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962490
Source datasetuspto-grants-1999_10
ORD IDord-09c45f5a28e74042986b98be015b6396
Source noteuspto-grants-1999_10