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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68328Generated: October 25, 2026

Water → Ethyl 3-(octahydroquinolin-1-yl)-3-oxopropionate

https://huagongshe.com/reaction/68328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantDecahydroquinolineHCID 92911—
ReactantEthyl 3-chloro-3-oxopropionateHCID 118931—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-(octahydroquinolin-1-yl)-3-oxopropionateHCID 6679456978.9%

Reaction Steps

3.38 mL of Et3N and 1.44 mL (11 mmol) of ethyl 3-chloro-3-oxopropionate are added to a solution of 1.5 mL (10 mmol) of decahydroquinoline in 100 mL of AcOEt. The resulting solution is kept under stirring at reflux for 10 h. Then water is added and the organic phase is separated, the aqueous phase is extracted once again with AcOEt. The organic phases are pooled and they are first washed with 5% solution of NaHCO3 and subsequently with brine, they are dried over anhydrous Na2SO4, they are filtered and the solvent is evaporated under reduced pressure. 2.0 g of a yellow oil are obtained. It is identified as intermediate IIIa.1. Method A: tr: 6.76 min; m/z: 268.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822452B2
Source datasetuspto-grants-2014_09
ORD IDord-e6a5c0325d5a4f4c8690b3127b1584ef
Source noteuspto-grants-2014_09