HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726133Generated: October 30, 2026
Water → 17beta-Carboxy-6-t-butoxycarbonyl-6-azaandrost-4-en-3-one
https://huagongshe.com/reaction/726133
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | 17beta-Carbomethoxy-6-t-butoxycarbonyl-6-azaandrost-4-en-3-one | HCID 10002872 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 17beta-Carboxy-6-t-butoxycarbonyl-6-azaandrost-4-en-3-one | HCID 10002048 | — |
Reaction Steps
A solution of 17β-carbomethoxy-6-t-butoxycarbonyl-6-azaandrost-4-en-3-one (15.4 g, 36 mmol), from part E, in dioxane (150 mL) and water (100 mL) is treated with LiOH.H2O (3.31 g, 79 mmol) and stirred overnight in a water bath. The reaction is poured into saturated aqueous NaHSO4 (150 mL), extracted with methylene chloride (3×100 mL), extracts washed with saturated aqueous NaCl, dried over MgSO4 and concentrated to a volume of 100 mL. At this point crystals begin to form and 2:1 hexanes/ethyl acetate (50 mL) is added, the mixture triturated, cooled to room temperature and 17β-carboxy-6-t-butoxycarbonyl-6-azaandrost-4-en-3-one collected as a fluffy white powder; yield: 9.44 g (63%); m.p. 215°-216° C. Anal. Calcd. for C24H35NO5.1/4H2O; C, 68.30; H, 8.48; N, 3.32. Found: C, 68.45; H, 8.41; N, 3.28.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05708001 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-35ceb399dcc7456b892caae04507d25f |
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| Source note | uspto-grants-1998_01 |
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