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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385108Generated: October 30, 2026

Formaldehyde → HCID 68109166, compound

https://huagongshe.com/reaction/385108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2-AminothiophenolHCID 8713—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzothiazolineHCID 96588—
ReactantHCID 86668173HCID 86668173—
SolventDichloromethaneHCID 6344—
ProductHCID 68109166HCID 68109166—

Reaction Steps

2,3-dihydro-1,3-benzothiazole synthesized from 2-aminobenzenethiol (346 mg) and 37% formalin (0.23 mL) in the same manner as in Example 1 was dissolved in dichloromethane (3 mL), and diisopropylethylamine (0.63 mL) and 4-benzyloxy-3-methoxy-5-trifluoromethylbenzoyl chloride (657 mg) were added to the solution, and then the mixture was stirred at room temperature for 1 hour. 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=6:1) to obtain the title compound (578 mg) as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367843B2
Source datasetuspto-grants-2013_02
ORD IDord-31f0cd90b56b4345b97bab2a6807f5f7
Source noteuspto-grants-2013_02