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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551541Generated: October 27, 2026

Water → 2-(7-Bromo-3-isoquinolinyl)ethyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/551541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant2-(7-Bromo-3-isoquinolinyl)ethanolHCID 21043927—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-(7-Bromo-3-isoquinolinyl)ethyl 4-methylbenzenesulfonateHCID 86592226—

Reaction Steps

The product from Example 52E (0.51 g, 2.0 mmol), tosyl chloride (0.68 g, 3.6 mmol), triethylamine (0.55 g, 5.4 mmol), and DMAP (25 mg, 0.2 mmol) were combined in dichloromethane (20 mL) and stirred at room temperature for 6 hours. The mixture was treated with water (0.5 mL), stirred for 2 hours, and then treated with additional water (15 mL). The organic layer was separated, washed with aqueous sodium chloride solution (10 mL, 10%), evaporated in vacuo, and the residue was azeotroped with heptane (15 mL) to provide the title compound which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947711B2
Source datasetuspto-grants-2011_05
ORD IDord-43575af23dca42359c81398e9d04f98f
Source noteuspto-grants-2011_05