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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059164Generated: October 25, 2026

17-Hydroxyprogesterone → Hydroxyprogesterone Impurity 14

https://huagongshe.com/reaction/2059164

Reaction equation

Participants

RoleNameHCIDCharge
Reactant17-HydroxyprogesteroneHCID 6238—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium AcetateHCID 517045—
SolventChloroformHCID 6212—
SolventDiethoxymethaneHCID 10024—
ProductHydroxyprogesterone Impurity 14HCID 1106784381.2%

Reaction Conditions

Temperature65 °C

Reaction Steps

A suspension of 1.0 g of sodium acetate in 30 ml of chloroform, 30 ml of formaldehyde diethylacetal, and 3.8 ml of phosphorus oxychloride is agitated in a two-necked flask for 1 hour at a bath temperature of 65° C. and then combined with 1.0 g of 17α-hydroxyprogesterone. The mixture is stirred for 1.5 hours at 65° C., cooled to room temperature, and under vigorous agitation a saturated soda solution is added dropwise until alkaline reaction occurs. The organic phase is separated, washed neutral with water, dried over sodium sulfate, and concentrated under vacuum. The crude product is purified on 220 g of silica gel with a methylene chloride/acetone gradient (0-12% acetone), thus obtaining 842 mg of 17α-hydroxy-6-methylene-4-pregnene-3,20-dione, mp 218°-220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04322349
Source datasetuspto-grants-1982_03
ORD IDord-9356e66c12e44ed9ae857b5fded72a1e
Source noteuspto-grants-1982_03