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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814180Generated: November 3, 2026

(6-Hydroxy-5-methyl-benzo[b]thiophen-3-yl)-acetic acid methyl ester → {5-Methyl-6-[2-(4-trifluoromethyl-benzyloxy)-benzyloxy]-benzo[b]-thiophen-3-yl}-acetic acid

https://huagongshe.com/reaction/1814180

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Hydroxy-5-methyl-benzo[b]thiophen-3-yl)-acetic acid methyl esterHCID 20770860—
Reactant(7-Hydroxy-benzo[b]thiophen-3-yl)acetic acid methyl esterHCID 20770870—
Reactant[2-(4-Trifluoromethyl-benzyloxy)-phenyl]-methanolHCID 22279996—
Product{5-Methyl-6-[2-(4-trifluoromethyl-benzyloxy)-benzyloxy]-benzo[b]-thiophen-3-yl}-acetic acidHCID 2250475043%

Reaction Steps

The title compound was prepared using compound 78C from the preceding step and compound 7A in a manner analogous to compound 77B. Thus, recrystallization from methanol afforded 0.42 g (43% yield) of the title compound as a cream-colored powder, mp 108-109° C. Calc for C27H23F3O4S: C, 64.79; H, 4.63; found: C, 64.64; H, 4.46. Step 5. Preparation of {5-Methyl-6-[2-(4-trifluoromethyl-benzyloxy)-benzyloxy]-benzo[b]thiophen-3-yl}-acetic acid (Compound 78)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875780B2
Source datasetuspto-grants-2005_04
ORD IDord-7b6c73ab37a743028c4cebd5a6ac4a83
Source noteuspto-grants-2005_04