HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23361Generated: October 25, 2026
Acetic Acid → 2-Methoxyestra-1,3,5(10),14-tetraen-3,17beta-diol
https://huagongshe.com/reaction/23361
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Methoxy-3,17-diacetoxyestra-1,3,5(10),14,16-pentaene | HCID 11326531 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 2-Methoxyestra-1,3,5(10),14-tetraen-3,17beta-diol | HCID 9839305 | — |
Reaction Steps
A solution of the diacetate (17) (0.08 g, 0.21 mmol) in ethanol (5 mL) and THF (3 mL) was cooled to 0° C. in an ice bath. A solution of sodium borohydride (0.05 g, 1.32 mmol) in ethanol/water (10:3, 5 mL) was cooled to 0° C. in an ice bath and added to the steroid solution. The reaction mixture was stirred at 0° C. for 1 h., then allowed to warm to room temperature and stirred overnight. After that time, the reaction was diluted with water (20 mL) and neutralized with glacial acetic acid. The organic solvents were removed in vacuo under a stream of nitrogen, the residue was diluted with water (50 mL) and extracted with methylene chloride (3×). The organic fractions were washed with water (2×), brine (1×), filtered through sodium sulfate, combined and concentrated in vacuo. The residue was triturated with ether to give the pure product (18) (0.035 g, 55.7%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852710B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-8495cdd51900489598f5fe670caee2fa |
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| Source note | uspto-grants-2005_02 |
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