HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059164Generated: October 25, 2026
17-Hydroxyprogesterone → Hydroxyprogesterone Impurity 14
https://huagongshe.com/reaction/2059164
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 17-Hydroxyprogesterone | HCID 6238 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Diethoxymethane | HCID 10024 | — |
| Product | Hydroxyprogesterone Impurity 14 | HCID 11067843 | 81.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04322349 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-9356e66c12e44ed9ae857b5fded72a1e |
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| Source note | uspto-grants-1982_03 |
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