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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270619Generated: October 31, 2026

Acetone → HCID 66931861, compound

https://huagongshe.com/reaction/270619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium ChlorideHCID 5234—
ReactantSodium borohydrideHCID 4311764—
ReactantEstradiene dione-3-ketaHCID 7076399—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
ProductHCID 66931861HCID 66931861—

Reaction Conditions

Temperature2 °C

Reaction Steps

Sodium borohydride (MW=37.8; 18.9 g; 500 mmol) in solution in 0.5 N sodium hydroxide (100 ml) is introduced, over approximately 5 min at around 2° C., into a suspension of 3,3-ethylenedioxyestra-5(10), 9(11)-dien-17-one (MW=314.4; 100 g; 318 mmol) in methanol (1 liter). The mixture is stirred for 2 h at around 2° C. and then acetone (100 ml) is introduced over approximately 15 min at around 5° C. The mixture is stirred for 1 h and the medium is run, at around 20° C., into a stirred mixture of water (2 liters), sodium chloride (500 g) and ethyl acetate (400 ml). The mixture is separated by settling out and the aqueous phase is re-extracted with ethyl acetate. The combined organic phases are washed with water, dried over sodium sulfate and concentrated at normal pressure to 500 ml. The distillation is continued while maintaining the volume constant by gradual introduction of 1,2-dimethoxyethane (DME). The temperature at the end of exchange is 83° C. The solution is used as it is in the subsequent stage, but a dry extract results in the expected product (resin). C20H28O3; MW=316.4:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449572B2
Source datasetuspto-grants-2008_11
ORD IDord-dfdaaec6bcf740a796cb532f5b622020
Source noteuspto-grants-2008_11