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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877995Generated: October 31, 2026

Acetone → HCID 68489938, compound

https://huagongshe.com/reaction/1877995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantOzoneHCID 24823—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68489914HCID 68489914—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 68489938HCID 68489938—

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Chloro-4-cyclopropyl-4-vinyl-1,4-dihydro-2H-3,1-benzoxazin-2-one (590 mg, 2.36 mmol) was dissolved in dichloromethane (2.5 mL) and methanol (2.5 mL), and the resulting solution was stirred at −78° C. in an ozone atmospher. After it was confirmed by thin-layer chromatography that the raw materials disappeared, the ozone atmospher was replaced by a nitrogen atmospher, and the solution was stirred for 5 minutes. The temperature of the reaction solution was raised to 0° C., and sodium borohydride (26.8 mg, 7.1 mmol) was added thereto. The reaction solution was stirred at 0° C. for 30 minutes, and then, acetone was added thereto to stop the reaction. After the solvent was evaporated under reduced pressure, water (50 mL) and 1 N hydrochloric acid were added to the residue and the pH thereof was adjusted to about 4, and then, the solution was stirred at room temperature. The resulting white solid was collected by filtration, washed with water and then dried under reduced pressure, whereby the objective compound (487 mg, 81%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314094B2
Source datasetuspto-grants-2012_11
ORD IDord-b8086c323f66494b9a47427ca1501f5f
Source noteuspto-grants-2012_11