Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241381Generated: November 2, 2026

Ammonium Chloride → HCID 66884043, compound

https://huagongshe.com/reaction/241381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
ReactantN-(3,5-Dimethyl-1,2-benzoxazol-6-yl)acetamideHCID 21928234—
ReactantHCID 66883686HCID 66883686—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 66884043HCID 6688404350%

Reaction Steps

To a suspension of N-(3,5-dimethylbenzisoxazol-6-yl)acetamide (381 mg, 1.87 mmol) in anhydrous THF (15 mL) was added dropwise 2M LDA (2.3 mL, 4.6 mmol) for 30 min at −78° C. under N2 atmosphere. The mixture was stirred for 30 min at −78° C., to which a solution of 2-chloromethyl-3-isopropyl-6-(trifluoromethyl)benzothiophene (655 mg, 2.24 mmol) in THF (5.0 mL) was added dropwise for 30 min. The mixture was stirred for 2 h at the same temperature, and then warmed to room temperature. A saturated aqueous ammonium chloride and ethyl acetate were added to the reaction mixture. The organic layer was washed with water, brine, and dried over anhydrous sodium sulfate. After the solvent was removed under reduced pressure, the residue was purified by silica gel column chromatography (hexane/ethyl acetate, 1:1) to give the titled compound as a pale yellow crystal (426 mg, yield. 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648208B2
Source datasetuspto-grants-2014_02
ORD IDord-5f56bf0539084eab983e0a691b15359a
Source noteuspto-grants-2014_02