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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385146Generated: October 30, 2026

Formaldehyde → 3-(3-Cyano-4-methoxy-5-trifluoromethoxybenzoyl)-2,3-dihydro-1,3-benzothiazole

https://huagongshe.com/reaction/385146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2-AminothiophenolHCID 8713—
ReactantBenzothiazolineHCID 96588—
Reactant3-Cyano-4-methoxy-5-trifluoromethoxybenzoyl chlorideHCID 86668183—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
Product3-(3-Cyano-4-methoxy-5-trifluoromethoxybenzoyl)-2,3-dihydro-1,3-benzothiazoleHCID 68109583—

Reaction Steps

2,3-dihydro-1,3-benzothiazole synthesized from 2-aminobenzenethiol (359 mg) and 37% formalin (0.24 mL) in the same manner as in Example 1 was dissolved in chloroform (10 mL), and triethylamine (0.80 mL) and 3-cyano-4-methoxy-5-trifluoromethoxybenzoyl chloride were added to the solution, and then the mixture was stirred at room temperature for 17 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 used for the synthesis of (j).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367843B2
Source datasetuspto-grants-2013_02
ORD IDord-43edb84109e443a6af6acbfc0a1953fc
Source noteuspto-grants-2013_02