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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12118Generated: October 30, 2026

Dichloromethane → HCID 11703849, compound

https://huagongshe.com/reaction/12118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 22063467HCID 22063467—
ReactantHCID 22063474HCID 22063474—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11703849HCID 11703849—

Reaction Conditions

Temperature0 °C

Reaction Steps

357 mg (1 mmol) of 6-benzyloxy-8-(2-ethoxy-2-hydroxy-acetyl)-4H-benzo[1,4]oxazin-3-one and 185 mg (1 mmol) of 2-(3,4-difluorophenyl)-1,1-dimethylethylamine are stirred for 30 minutes in 5 mL tetrahydrofuran at ambient temperature. It is cooled to 0° C. and, under an argon atmosphere, 1.5 mL of a 2 molar solution of lithium borohydride in tetrahydrofuran is added dropwise. The mixture is stirred for 30 minutes at ambient temperature, combined with 10 mL dichloromethane, and 3 mL water, stirred for a further hour and then filtered through an EXTRELUT® column. The eluate containing the ethanol amine is freed from solvent. The residue is dissolved in methanol and hydrogenated with palladium on charcoal (10%) as catalyst at 2.5 bar and ambient temperature. Then the catalyst is separated off and the crude product is purified by chromatography. White solid. Yield: 31 mg (6%, trifluoroethyl acetate); mass spectroscopy: [M+H]+=393.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727984B2
Source datasetuspto-grants-2010_06
ORD IDord-4441e79696ac40c1bf0f8abad85e67ee
Source noteuspto-grants-2010_06