HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963185Generated: October 30, 2026
Hydrochloric Acid → HCID 86752725, compound
https://huagongshe.com/reaction/963185
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 10541223 | HCID 10541223 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86752725 | HCID 86752725 | 78% |
Reaction Steps
To a suspension of magnesium (0.110 g 4.5 mmol) in THF (1.0 mL) was added bromoethane (0.50 mL, 6.6 mmol) dissolved in THF (1.0 mL) at room temperature. 3-Hydroxy-17β-methoxyestra-1,3,5(10)-triene (41, 0.258 g, 0.90 mmol; synthesized by the method of Coombs et al., Steroids 6(6):841-844 (1965)), dissolved in THF (3.0 mL) was added to the reaction mixture, and stirring continued for 30 min. The solvent was removed at reduced pressure, and to the residue were added benzene (10 mL, hexamethylphosphoric triamide (0.40 mL, 2.1 mmol) and paraformaldehyde (0.370 g). Stirring was continued for 2 h at 80° C. After the reaction mixture was cooled to room temperature, 5N HCl (5.0 mL) was added and the mixture extracted with EtOAc. The combined organic layers were washed with H2O, then with saturated aqueous NaCl, and dried (Na2SO4). The desiccant was filtered and the solvent was evaporated at reduced pressure. The residue was purified by column chromatography (silica gel) using n-hexane:AcOEt (10:1→8:1, v/v) to afford 0.221 g of 42 (78% yield), m.p. 120°-121° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05763432 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-6babae78deb14875bfa4874647bc1932 |
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| Source note | uspto-grants-1998_06 |
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