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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385156Generated: October 29, 2026

Formaldehyde → HCID 68108693, compound

https://huagongshe.com/reaction/385156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2-AminothiophenolHCID 8713—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzothiazolineHCID 96588—
ReactantHCID 86668184HCID 86668184—
SolventDichloromethaneHCID 6344—
ProductHCID 68108693HCID 68108693—

Reaction Steps

2,3-dihydro-1,3-benzothiazole synthesized from 2-aminobenzenethiol (278 mg) and 37% formalin (0.18 mL) in the same manner as in Example 1 was dissolved in dichloromethane (6.5 mL), and diisopropylethylamine (0.50 mL) and 3-chloro-4-methoxy-5-trifluoromethoxybenzoyl chloride (436 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 used for the synthesis of (k).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367843B2
Source datasetuspto-grants-2013_02
ORD IDord-93f3557f041a47548bc951987cab0c63
Source noteuspto-grants-2013_02