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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077589Generated: October 31, 2026

Water → 17beta-Carboxy-6-t-butylcarboxy-6-azaandrost-4-en-3-one

https://huagongshe.com/reaction/1077589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantSodium BisulfateHCID 516919—
Reactant17beta-Carbomethoxy-6-t-butylcarboxy-6-azaandrost-4-en-3-oneHCID 86749035—
Solvent1,4-DioxaneHCID 31275—
Product17beta-Carboxy-6-t-butylcarboxy-6-azaandrost-4-en-3-oneHCID 86749034—

Reaction Steps

A solution of 17β-carbomethoxy-6-t-butylcarboxy-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 on 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-butylcarboxy-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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05543406
Source datasetuspto-grants-1996_08
ORD IDord-e303bbe3491945168c7a5fbe38e788f0
Source noteuspto-grants-1996_08