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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503109Generated: October 30, 2026

Benzothiazole → 1,3-Benzothiazol-2-yl[5-(dimethoxymethyl)-2-fluorophenyl]methanol

https://huagongshe.com/reaction/503109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazoleHCID 7222—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-(Dimethoxymethyl)-2-fluorobenzaldehydeHCID 22260704—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1,3-Benzothiazol-2-yl[5-(dimethoxymethyl)-2-fluorophenyl]methanolHCID 2226084879.3%

Reaction Steps

A total of 1.08 g of benzothiazole was dissolved in 15 ml of dry tetrahydrofuran. After cooling to −78° C. in an atmosphere of nitrogen gas, 6.4 ml of 1.56 M solution of n-butyllithium in hexane was added. After stirring for 5 minutes, 8 ml of a solution of 1.35 g of 5-(dimethoxymethyl)-2-fluorobenzaldehyde in dry tetrahydrofuran was added, followed by stirring for 10 minutes. To the reaction mixture was added aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate for two times. The organic layer was washed with water, dried over anhydrous magnesium sulfate and the solvent was evaporated. The residue was purified and separated by silica gel column chromatography (ethyl acetate:hexane=3:7), to give 1.8 g of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776890B2
Source datasetuspto-grants-2010_08
ORD IDord-7c17faf0ce1a40208dd88888a9a8673b
Source noteuspto-grants-2010_08