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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454314Generated: November 1, 2026

Water → [(2R)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methyl4-bromobenzenesulfonate

https://huagongshe.com/reaction/1454314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
ReactantTriethylamineHCID 8471—
Reactant[(2S)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]-methanolHCID 11183845—
Catalyst2-DimethylaminopyridineHCID 21885—
SolventTolueneHCID 1140—
SolventIsopropanolHCID 3776—
Product[(2R)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methyl4-bromobenzenesulfonateHCID 2062476276.9%

Reaction Steps

A solution of [(2S)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]-methanol (4.0 g, 17.3 mmol), brosyl chloride (4.86 g, 19.0 mmol), dimethylamino pyridine (20 mg, 0.16 mmol) and triethylamine (3.62 mL, 25.8 mmol) in toluene (40 mL) was stirred at 60° C. for 6 h. The reaction mixture was cooled to room temperature then water (20 mL) was added. After 30 min, the two layers were separated. The organic layer was extracted with 8% NaHCO3 (20 mL) and H2O (20 mL), dried over Na2SO4, filtered and concentrated in vacuo. The solid obtained was dissolved in isopropyl alcohol (50 mL) and toluene (10 mL) at 80° C., cooled to room temperature over 1 h then filtered, washed with (5:1) IPA: toluene (2×5 mL) and dried in a vacuum oven to give 5.99 g (76.9%) of the title compound as an off-white solid. 13C NMR (CDCl3) δ 157.9, 144.3, 138.1, 134.7, 132.9, 129.7, 129.6, 129.0, 122.4, 121.7, 121.3, 118.8, 70.7, 67.6, 64.5, 25.4

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07479500B2
Source datasetuspto-grants-2009_01
ORD IDord-75fa76d1cfc44589a5a09b6a09a3dd73
Source noteuspto-grants-2009_01