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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808756Generated: October 31, 2026

Water → 7-[O-(3-chloropropyl)oximino]-5-androstene-3beta,17beta-diol diacetate

https://huagongshe.com/reaction/1808756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Oximino-5-androstene-3beta,17beta-diol DiacetateHCID 86761753—
SolventMethyl Ethyl KetoneHCID 6569—
Product7-[O-(3-chloropropyl)oximino]-5-androstene-3beta,17beta-diol diacetateHCID 8676175458.82%

Reaction Steps

A mixture of 7-oximino-5-androstene-3β,17β-diol diacetate (1 g, 2.48 mmol) and anhydrous potassium carbonate (2 g) was stirred and refluxed in ethyl methyl ketone (100 Ml) at 110° C. for 3 h. 1-Bromo-3-chloropropane (0.25 Ml, 2.48 mmol) was added to the reaction mixture and further refluxed for 20 h with continuous stirring. The completion of the reaction was monitored by TLC. The slurry was cooled, filtered and excess of solvent was removed under reduced pressure to obtain an oily residue. Iced water was added to the oily residue and it was allowed to stand overnight. The precipitate obtained was filtered, washed with water, dried and crystallized from pet-ether (60-80° C.) to afford 7-[O-(3-chloropropyl)oximino]-5-androstene-3β,17β-diol diacetate (23) (0.7 g, 58.82%), mp 155° C. (Decomp).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08361996B2
Source datasetuspto-grants-2013_01
ORD IDord-381c127beb7f45868c2e11246512e97c
Source noteuspto-grants-2013_01