HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868168Generated: November 1, 2026
Phosphorus oxychloride → HCID 13477372, compound
https://huagongshe.com/reaction/868168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 13477370 | HCID 13477370 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethoxymethane | HCID 8020 | — |
| Product | HCID 13477372 | HCID 13477372 | 57% |
Reaction Steps
A suspension of 10.0 g of sodium acetate in 300 ml of chloroform and 300 ml of formaldehyde dimethylacetal is stirred with 19 ml of phosphorus oxychloride for one hour at a bath temperature of 65° C. After adding 10.0 g of 17α-hydroxy-16β-methyl-4,9(11)-pregnadiene-3,20-dione, another 19 ml of phosphorus oxychloride is added dropwise and the reaction solution is stirred for another 6.5 hours at 65° C. The cooled-off solution is treated with such an amount of a saturated soda solution that the aqueous phase is made permanently alkaline. The organic phase is separated, washed neutral and concentrated after drying. The crude product is purified on 700 g of silica gel with a hexane-ethyl acetate gradient (0-50% ethyl acetate), thus isolating 5.9 g of 17α-hydroxy-16β-methyl-6-methylene-4,9(11)-pregnadiene-3,20-dione, mp 157°-158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04777165 |
|---|
| Source dataset | uspto-grants-1988_10 |
|---|
| ORD ID | ord-aa06e7dc3f4f466ca3129adcbfcb0df6 |
|---|
| Source note | uspto-grants-1988_10 |
|---|