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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256318Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 19029354, compound

https://huagongshe.com/reaction/2256318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2-[3-(3,4-Dichlorophenyl)-5-hydroxy-1-oxopentyl]-1,2,3,4-tetrahydroisoquinolineHCID 19029390—
SolventDichloromethaneHCID 6344—
ProductHCID 19029354HCID 1902935480.4%

Reaction Steps

A solution of oxalyl chloride (0.460 mL) in CH2Cl2 (20 mL) was cooled to -78° C. whereupon DMSO (0.749 mL) was added dropwise over 15 mins. This mixture was stirred for 15 minutes. Whereupon a CH2Cl2 (10 mL) solution of 2-[3-(3,4-dichlorophenyl)-5-hydroxy-1-oxopentyl]-1,2,3,4-tetrahydroisoquinoline (1.0 g) was added over 20 minutes. The mixture was stirred for 30 minutes and then treated with Et3N (3 mL) and stirred for an additional 30 minutes at -78° C., followed by 1.5 hours at room temperature. The reaction mixture was quenched with water and diluted with CH2Cl2 (100 mL). The organic fraction was separated, washed sequentially with 1N HCl (1×50 mL), sat. NaHCO3 (1×50 mL) and brine (1×50 mL), dried over MgSO4, filtered and concentrated under reduced pressure to yield an oil. Silica gel chromatography eluting with 5-15% EtOAc/Hex gave the title compound (800 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654316
Source datasetuspto-grants-1997_08
ORD IDord-9095a4522cc24d5e9609bc3b7fe2a74a
Source noteuspto-grants-1997_08