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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405068Generated: October 30, 2026

Acetic Acid → HCID 86676408, compound

https://huagongshe.com/reaction/405068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(2-Amino-1-(3-pyridyl)ethyl)dimethylamineHCID 3864338—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-butyl 4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-formyl-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]chrysen-9-yl)benzoateHCID 86676397—
Solvent1,2-DichloroethaneHCID 11—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86676408HCID 86676408—

Reaction Steps

To a solution of tert-butyl 4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-formyl-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]chrysen-9-yl)benzoate (0.1 g, 0.167 mmol) in DCE (2 ml) was added acetic acid (0.019 ml, 0.334 mmol) and (2-Amino-1-(3-pyridyl)ethyl)dimethylamine (0.055 g, 0.334 mmol). The mixture was stirred at rt for 2 h then sodium triacetoxyborohydride (0.177 g, 0.835 mmol) was added and it was stirred at rt for three days. The mixture was diluted with 7 ml of sat. NaHCO3 and was extracted with dichloromethane (3×7 ml). The combined organic layers were dried with Na2SO4. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure. The crude product was used in the next step with no additional purification. LCMS: m/e 748.3 (M+H)+, 3.47 min (method 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748415B2
Source datasetuspto-grants-2014_06
ORD IDord-8e762d476f2a41a59d27cbed3da6999e
Source noteuspto-grants-2014_06