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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52459Generated: October 25, 2026

Triethylamine → N-ethoxalylindoline

https://huagongshe.com/reaction/52459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIndolineHCID 10328—
ReactantEthoxalyl chlorideHCID 20884—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
ProductN-ethoxalylindolineHCID 1581489108.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of indoline (2.0 g, 16.8 mmol) and triethylamine (5 mL) in dichloromethane (30 mL) was added slowly ethyl chlorooxalate (2.3 mL, 20.1 mmol) at 0° C. The mixture was stirred for 10 min at 0° C. and then for 1 h at room temperature. Brine was added and organic layer was separated. The organic layer was washed with diluted aqueous hydrochloric acid and successively brine, dried over magnesium sulfate, and concentrated to give 4.0 g of N-ethoxalylindoline (100%): 1H NMR (270 MHz, CDCl3) δ8.18 (dd, 1H, J=8, 1 Hz), 7.22 (m, 2H), 7.10 (dd, 1H, J=8, 1 Hz), 4.38 (q, 2H, J=7 Hz), 4.22 (t, 2H, J=8 Hz), 3.20 (t, 2H, J=8 Hz), 1.40 (t, 3H, J=7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616586
Source datasetuspto-grants-1997_04
ORD IDord-7502193e0e7e4d59a65bd231224295fd
Source noteuspto-grants-1997_04