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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942412Generated: November 3, 2026

Triethylamine → N-(indan-2-yl)-5-oxopentanamide

https://huagongshe.com/reaction/1942412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantN-(indan-2-yl)-5-hydroxypentanamideHCID 66937348—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
ProductN-(indan-2-yl)-5-oxopentanamideHCID 86651316—

Reaction Steps

A solution of 1.11 mL (12.8 mmol) oxalyl chloride in 35 mL of dichloromethane is cooled to −80° C. under argon atmosphere. 2.33 mL (32.7 mmol) of dimethylsulfoxide in 9.33 mL of dichloromethane is introduced dropwise over 10 minutes. After 5 minutes a solution of 1.63 g (7 mmol) N-(2,3-dihydro-1H-inden-2-yl)-5-hydroxypentanamide in 8 mL dichloromethane and 2 mL dimethylsulfoxide is added over the course of 10 minutes. The reaction mixture is stirred for another hour at −80° C. before 5 mL of triethylamine is added and the mixture is allowed to warm up to room temperature. 50 mL of saturated brine solution is added for hydrolysis. The organic phase is separated, extracted three times with a saturated solution of sodium chloride, dried over sodium sulfate and the solvent is evaporated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389555B2
Source datasetuspto-grants-2013_03
ORD IDord-b2d19534dd624f0aa8113c3699c51111
Source noteuspto-grants-2013_03