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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493989Generated: October 30, 2026

Acetic Acid → HCID 67073393, compound

https://huagongshe.com/reaction/493989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantIsopropyl iodideHCID 6362—
ReactantHCID 67073446HCID 67073446—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 67073393HCID 6707339359%

Reaction Steps

To a mixture of 5-((S)-1-benzyl-pyrrolidin-3-yloxy)-1H-indole-2-carboxylic acid ethyl ester (18.0 g, 1.0 eq.) and acetic acid (28 mL, 10 eq.) in ethanol (500 mL) was added palladium on activated charcoal (10% in mass, 2.0 g, 0.04 eq.) and the reaction vessel was flushed with hydrogen (1 Atm). The reaction mixture was stirred 18 h at room temperature and then filtered off and concentrated in vacuo. The residue (28.4 g) was dissolved in dimethylformamide (500 mL) and potassium carbonate was added. The mixture was stirred 15 min at room temperature. Then 2-iodopropane (42 g, 5.0 eq.) was added and the mixture was stirred 4 h at 50° C. The reaction mixture was filtered off and the filtrate was evaporated in vacuo. The residue was dissolved in acetone, filtered and the filtrate was evaporated in vacuo then purified on silica eluting with dichloromethane/methanol/ammoniac. One fraction was isolated and dried in vacuo, to yield 9.3 g (59%) of the desired product as light brown solid. MS (m/e): 317.4 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538101B2
Source datasetuspto-grants-2009_05
ORD IDord-80392c0832804e07a176d4189e6b9f5e
Source noteuspto-grants-2009_05