Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073733Generated: October 30, 2026

Dichloromethane → HCID 15053682, compound

https://huagongshe.com/reaction/1073733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantIndolineHCID 10328—
Reactant4-[(Diethoxyphosphoryl)-methyl]benzoyl chlorideHCID 10446973—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 15053682HCID 15053682—

Reaction Steps

1.80 Grams (15 mM) of indoline, 1.82 g (18 mM) of triethylamine and 0.37 g (3 mM) of 4-dimethylaminopyridine were dissolved in 30 ml of dry dichloroethane, to this solution was added dropwise slowly 30 ml of dry dichloromethane solution with 5.21 g (15 mM) of 4-diethoxyphosphinoylmethylbenzoyl chloride at 0° C. with stirring. After the stirring was continued for 10 hours at room temperature, 50 ml of water was added to the reaction mixture and extracted with chloroform. The extracts were dried over anhydrous sodium sulfate, and concentrated. The residue thus obtained was purified by means of a silica gel column chromatography (eluted with chloroform:ethyl acetate=1:1). The crude crystals were recrystallized from benzene-n-hexane to yield 3.90 g of 1-(4-diethoxyphosphinoylmethylbenzoyl)indoline as colorless crystals Melting point 93.0°-94.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971957
Source datasetuspto-grants-1990_11
ORD IDord-12790a64000947c4be33f0ae15f25eec
Source noteuspto-grants-1990_11