Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638823Generated: November 1, 2026

Sodium Bicarbonate → 7,8-Difluoro-2,3-dihydro-3-methyl-4H-(1,4)benzoxazine

https://huagongshe.com/reaction/1638823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13192919HCID 13192919—
SolventChloroformHCID 6212—
Product7,8-Difluoro-2,3-dihydro-3-methyl-4H-(1,4)benzoxazineHCID 1021971866.2%

Reaction Steps

To the ethyl acetate layer were added 0.47 g of sodium borohydride and 2 ml of ethanol, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was washed twice with 10 ml portions of 5% aqueous citric acid solution and once with 10 ml of dilute aqueous ammonia (the same as mentioned hereinbefore), and dried over anhydrous magnesium sulfate. The desiccant was filtered off and to the solution was added with 0.72 ml of concentrated hydrochloric acid with stirring. After cooling with ice-water, the resulting crystals were collected by filtration and washed with cold ethyl acetate to give 1.236 g of 7,8-difluoro-3-methyl-3,4-dihydro-2H-[1,4]benzoxazine hydrochloride as colorless crystals. Optical purity: 1.0% e.e., (S), 3S:3R =1.02:1.00. In 10 ml of chloroform was suspended 1.078 g of the above hydrochloride and to the suspension was added 10 ml of 5% aqueous sodium hydrogen carbonate solution with stirring. The chloroform layer was washed with water and dried over anhydrous magnesium sulfate. Then, the desiccant was filtered off and the solvent was distilled off under reduced pressure. The residue was dissolved in 1 ml of methanol, followed by addition of 5 ml of 50% aqueous methanol. After cooling with ice-water, the resulting crystals were collected by filtration to give 0.596 g of the title compound (yield: 60.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880926
Source datasetuspto-grants-1989_11
ORD IDord-d5b2dc789ae74fdb888d1f6dc4c9ae3d
Source noteuspto-grants-1989_11