HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456006Generated: October 31, 2026
Nitrogen → Methyl (3β)-3-hydroxy-7-oxochol-5-en-24-oate
https://huagongshe.com/reaction/1456006
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23250093 | HCID 23250093 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl (3β)-3-hydroxy-7-oxochol-5-en-24-oate | HCID 23250094 | — |
Reaction Steps
To a suspension of finely ground K2CO3 (3.45 g , 25 mmoles) in 250 ml of methanol was added methyl 3β-acetoxy-7-oxochol-5-en-24-oate (1) (11.1 g, 25 mmoles). After stirring at 450° for 15 min in a N2 atmosphere, most of the methanol was removed in vacuo from the clear brown reaction mixture. The residue was suspended in H2O and extracted three times with CH2Cl2. The combined extracts were washed with H2O twice and saturated brine and dried with MgSO4. Evaporation in vacuo gave 10.1 g of nearly pure 2 as a pale yellow solid. The nuclear magnetic resonance data for this and subsequent Examples was taken at 400 MHz in CDCl3 : δ 0.68 (s, 3H, 18-Me); 0.94 (d, 3H, 20-Me); 1.21 (s, 3H, 19-Me); 3.66 (s, 3H, CO2Me); 3.68 (m, 1H, 3-H); 5.70 (s, 1H, 6-H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05843953 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-53946114295e4e8e87bcdc95170d2345 |
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| Source note | uspto-grants-1998_12 |
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