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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069476Generated: October 29, 2026

Triethylamine → 2-(Methanesulfonyloxymethyl)-6-methyl-nitrobenzene

https://huagongshe.com/reaction/1069476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-Methyl-2-nitrobenzenemethanolHCID 561989—
SolventDichloromethaneHCID 6344—
Product2-(Methanesulfonyloxymethyl)-6-methyl-nitrobenzeneHCID 1576695697.9%

Reaction Steps

At 10-15° C., 27 g (0.23 mol) of methanesulfonyl chloride dissolved in 20 ml of CH2Cl2 is dripped into a mixture of 34 g (0.2 mol) of 3-methyl-2-nitrobenzyl alcohol and 27 g (0.27 mol) of triethylamine in 100 ml of CH2Cl2. The reaction mixture is stirred for 1 hour at room temperature and is then extracted with water. The organic phase is dried over MgSO4 and evaporated down. There is obtained as residue 48 g of the title compound as a yellow oil, containing about 10% of the corresponding benzyl chloride as impurity. The crude product is used for the next reaction without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06252083B1
Source datasetuspto-grants-2001_06
ORD IDord-10634ab235344e1d8cb90a9a5c93b753
Source noteuspto-grants-2001_06