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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773035Generated: November 2, 2026

Hydrochloric Acid → HCID 86731493, compound

https://huagongshe.com/reaction/1773035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant(1R,3aS,5aR,5bR,7aR,11aS,13aR,13bR)-benzyl 9-((E)-3-ethoxy-3-oxoprop-1-enyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysene-3a-carboxylateHCID 86731492—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86731493HCID 86731493105%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (1R,3aS,5aR,5bR,7aR,11aS,13aR,13bR)-benzyl 9-((E)-3-ethoxy-3-oxoprop-1-enyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysene-3a-carboxylate (20 mg, 0.032 mmol) and 10 N sodium hydroxide (0.032 mL, 0.319 mmol) in dioxane (0.5 mL) and water (0.5 mL) was heated at 100° C. for 3 hours. The reaction mixture was neutralized with 1N HCl to pH=6 and extracted with ethyl acetate (3×4 mL). The extracts were combined, dried over sodium sulfate, filtered and concentrated under reduced pressure to provide the title compound (20 mg, 105%). This material was used in the next step without further purification. LCMS: m/e 597.68 (M−H)−, 2.50 min (method 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249180B2
Source datasetuspto-grants-2016_02
ORD IDord-8ab7a39c5e504f02b0a6de21d88708f6
Source noteuspto-grants-2016_02