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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585514Generated: November 2, 2026

HCID 22872549, compound → HCID 86750802, compound

https://huagongshe.com/reaction/1585514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22872549HCID 22872549—
ReactantHCID 54041341HCID 54041341—
CatalystSilver(II) oxideHCID 92152—
SolventPyridineHCID 1049—
ProductHCID 86750802HCID 86750802—

Reaction Steps

The following procedure is a variation of that described in Helv. Chim. Act., 1953, 36, 1241. (3β,5α,11α,12β,25R)-11,23-dibromospirostan-3,12-diol (18.08 g) was dissolved in pyridine (500 mL) at room temperature and treated with silver oxide (70.0 g). The resulting mixture was stirred in the dark for 71 hours. The mixture was filtered and the solid washed with ether and then chloroform. These washes were combined with the filtrate and concentrated. The resulting solid was purified by flash chromatography (1:1 hexane:ethyl acetate) to give 12.2 g of a 1:1 mixture of the title compound and (3β,5α,25R)-23-bromospirostan-3-ol-12-one. Further chromatography (7:3 hexane:ethyl acetate) provides pure title compound. (3β,5α,11β,12α,25R)-23-bromo-12-(trichloroacetoxy)spirostan-3,11 -diol: Using the procedure described in J. Chem. Soc., 1956, 4330, (3β,5α, 11β,12β,25R)-23-bromo-11,12-epoxyspirostan-3-ol was treated with trichloroacetic acid in toluene at room temperature for 3 days to give the title compound. (3β,5α, 11β,12α,25R)-23-bromo-spirostan-3,11,12-triol: Using the procedure described in J. Chem. Soc., 1956, 4330, (3β,5α,11β,12α,25R)-23-bromo-12-(trichloroacetoxy)spirostan-3,11-diol was saponified with sodium hydroxide in water and ethanol to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939398
Source datasetuspto-grants-1999_08
ORD IDord-6c7d7c0fd37043198418bdebbcd288f3
Source noteuspto-grants-1999_08