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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602492Generated: November 1, 2026

Tetrahydrofuran → 3-(4,5,6,7-Tetrahydrobenzothiazol-2-ylmethoxy)benzoic acid

https://huagongshe.com/reaction/1602492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-(4,5,6,7-tetrahydrobenzothiazol-2-ylmethoxy)benzoateHCID 19611521—
SolventMethanolHCID 887—
Product3-(4,5,6,7-Tetrahydrobenzothiazol-2-ylmethoxy)benzoic acidHCID 1961157875%

Reaction Steps

A mixture of methyl 3-(4,5,6,7-tetrahydrobenzothiazol-2-ylmethoxy)benzoate (361 mg, 1.2 mmol), tetrahydrofuran (2 ml), methanol (2 ml) and 1 N sodium hydroxide (2 ml) was stirred at room temperature for 12 hours and then concentrated under reduced pressure. The resulting residue was dissolved in water and the solution was adjusted to pH 3 by adding 10% citric acid aqueous solution. Thereafter, the solid substance formed was collected by filtration, washed with water, and then dried under reduced pressure to give 3-(4,5,6,7-tetrahydrobenzothiazol-2-ylmethoxy)benzoic acid (257 mg, 0.89 mmol, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981559
Source datasetuspto-grants-1999_11
ORD IDord-a7e677c24d794a738ca9e02d5e8b4ac4
Source noteuspto-grants-1999_11