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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383021Generated: October 28, 2026

Chloroacetyl chloride → HCID 59396492, compound

https://huagongshe.com/reaction/2383021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 59396601HCID 59396601—
SolventTolueneHCID 1140—
ProductHCID 59396492HCID 59396492—

Reaction Steps

Chloroacetyl chloride (0.151 mL) was added to a solution of 1,1-diphenyl-1,2,3,4-tetrahydroisoquinoline (339 mg) and p-toluenesulfonate monohydrate (11.3 mg) in toluene (5 mL). The mixture was heated under reflux for 3 hours. The solvent was evaporated under reduced pressure, and EtOAc and an aqueous 1 M HCl solution were added to the residue. The organic layer was washed with water, a saturated aqueous sodium hydrogen carbonate solution, and saturated brine, dried over magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure to obtain 2-(chloroacetyl)-1,1-diphenyl-1,2,3,4-tetrahydroisoquinoline (452 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263607B2
Source datasetuspto-grants-2012_09
ORD IDord-ef722d5a99f54f4691ed642429c6ca81
Source noteuspto-grants-2012_09