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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497999Generated: November 3, 2026

Succinic anhydride → HCID 68281999, compound

https://huagongshe.com/reaction/1497999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinic anhydrideHCID 7922—
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Propanamine, 3-[(3b)-cholest-5-en-3-yloxy]-HCID 57358590—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68281999HCID 68281999114.9%

Reaction Steps

In a 2 L round-bottomed flask, 3-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yloxy)propan-1-amine (21.15 g, 47.7 mmol, Eq: 1.00) and Huenig's base (12.3 g, 16.6 ml, 95.3 mmol, Eq: 2.00) were combined with AcOEt (845 ml) to give a colorless solution. Dihydrofuran-2,5-dione (4.77 g, 47.7 mmol, Eq: 1.00) in THF (42 ml) was added and the reaction mixture was stirred at ambient temperature over night=>white suspension. All volatiles were removed i. v., the residue dissolved in CH2Cl2, the organic layer washed with NH4Cl and brine, dried over Na2SO4, and evaporated to dryness. The crude product was dissolved in CH3CN/H2O and lyophilized to yield 29.8 g of the title compound as fluffy powder. MS (ISP): (M−H) 542.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09198947B2
Source datasetuspto-grants-2015_12
ORD IDord-c33113f704ec4f229936d46f5218eab3
Source noteuspto-grants-2015_12