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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625140Generated: October 30, 2026

Succinic anhydride → HCID 68281999, compound

https://huagongshe.com/reaction/625140

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 μL 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 numberUS09301990B2
Source datasetuspto-grants-2016_04
ORD IDord-3a5c173a2ce94c38b5e3f0d2ef5d7ab5
Source noteuspto-grants-2016_04