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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234385Generated: October 30, 2026

3,4,5-Trimethoxybenzaldehyde → HCID 49962541, compound

https://huagongshe.com/reaction/234385

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 49962541HCID 49962541—

Reaction Steps

α-(2-benzo[b]thienyl)-3,4,5-trimethoxybenzyl 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 (1.7m, 9.7 mmoles, 5.7 mls) and 3,4,5-trimethoxybenzaldehyde (8.9 mmoles, 1.8 g) in THF (20 ml) yielded, after flash chromatography using 50% ethyl acetate/hexanes, 2.4 g (97%) of a yellow-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594021
Source datasetuspto-grants-1997_01
ORD IDord-bf3d8a8104194d6ab788bf02565ee542
Source noteuspto-grants-1997_01