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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116074Generated: October 31, 2026

4-Toluenesulfonyl chloride → (+/-)-(7-Nitro-2,3-dihydro-1-benzofuran-2-yl)methyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/2116074

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantDiisopropylethylamineHCID 81531—
Reactant(+/-)-(7-Nitro-2,3-dihydro-1-benzofuran-2-yl)methanolHCID 11063317—
SolventDichloromethaneHCID 6344—
Product(+/-)-(7-Nitro-2,3-dihydro-1-benzofuran-2-yl)methyl 4-methylbenzenesulfonateHCID 8659915594%

Reaction Steps

To a solution of (±)-(7-nitro-2,3-dihydro-1-benzofuran-2-yl)methanol (3.14 g, 16.09 mol) in dichloromethane (100 mL) was added diisopropylethyl amine (4.16 g, 32.18 mmol), N,N-dimethylaminopyridine (0.39 g, 3.2 mmol), and p-toluenesulfonyl chloride (4.6 g, 24.13 mmol) the reaction was allowed to stir at room temperature for 12 h. The reaction was diluted with dichloromethane (500 mL), washed with saturated aqueous sodium bicarbonate (200 mL), saturated aqueous sodium chloride (200 mL), dried (magnesium sulfate) and the solvent removed in vacuo to give a crude oil. Purification by flash column chromatography (silica, dichloromethane: hexanes 3:10) afforded 5.2 g (94%) of (±)-(7-nitro-2,3-dihydro-1-benzofuran-2-yl)methyl 4-methylbenzenesulfonate as off-white solid. mp 129-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435837B2
Source datasetuspto-grants-2008_10
ORD IDord-423c347516624bbfa48f9d5e2c0b7b91
Source noteuspto-grants-2008_10