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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385057Generated: October 31, 2026

Formaldehyde → HCID 68108936, compound

https://huagongshe.com/reaction/385057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2-AminothiophenolHCID 8713—
ReactantBenzothiazolineHCID 96588—
ReactantHCID 86668161HCID 86668161—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 68108936HCID 68108936—

Reaction Steps

2,3-dihydro-1,3-benzothiazole synthesized from 2-aminobenzenethiol (318 mg) and 37% formalin (0.21 mL) in the same manner as in Example 1 was dissolved in dichloromethane (6 mL), and triethylamine (0.71 mL) and 3-cyano-5-ethyl-4-methoxybenzoyl chloride (387 mg) were added to the solution, and then the mixture was stirred at room 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=6:1) to obtain the title compound (498 mg) as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367843B2
Source datasetuspto-grants-2013_02
ORD IDord-d2c8473b31e74e7986f924b11a215c6c
Source noteuspto-grants-2013_02