Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385116Generated: October 30, 2026

Formaldehyde → 3-(4-Benzyloxy-3-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole

https://huagongshe.com/reaction/385116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2-AminothiophenolHCID 8713—
ReactantBenzothiazolineHCID 96588—
Reactant4-Benzyloxy-3-trifluoromethylbenzoyl chlorideHCID 86668175—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
Product3-(4-Benzyloxy-3-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazoleHCID 68108976—

Reaction Steps

2,3-dihydro-1,3-benzothiazole synthesized from 2-aminobenzenethiol (282 mg) and 37% formalin (0.19 mL) in the same manner as in Example 1 was dissolved in chloroform (6 mL), and triethylamine (0.62 mL) and 4-benzyloxy-3-trifluoromethylbenzoyl chloride were added to the solution, and then the mixture was stirred at mom temperature for 1.5 hours. The solvent was distilled off under reduced pressure and water was added, and then the mixture was extracted with ethyl acetate. The organic layer was washed with 1N hydrochloric acid, 1N sodium hydroxide and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1) to obtain the title compound (356 mg) as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367843B2
Source datasetuspto-grants-2013_02
ORD IDord-20241d3e0d9f4098ac481fe66ad2b1ea
Source noteuspto-grants-2013_02