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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797634Generated: November 2, 2026

Thionyl Chloride → HCID 22175355, compound

https://huagongshe.com/reaction/1797634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22175847HCID 22175847—
SolventTolueneHCID 1140—
ProductHCID 22175355HCID 2217535589.8%

Reaction Steps

To a suspension of 6-benzyloxy-4-(4-chlorophenyl)-3-hydroxymethyl-2-isobutyl-1(2H)-isoquinolinone (4.25 g, 9.5 mmol) in toluene (50 ml) was added thionyl chloride (1.4 ml, 19 mmol). The obtained mixture was refluxed under heating for 2 h. The reaction mixture was poured into saturated aqueous sodium hydrogencarbonate solution and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 6-benzyloxy-3-chloromethyl-4-(4-chlorophenyl)-2-isobutyl-1(2H)-isoquinolinone (3.98 g, 89.8%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034039B2
Source datasetuspto-grants-2006_04
ORD IDord-cb5018f86a7246798d3777bf6adb59d5
Source noteuspto-grants-2006_04