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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360514Generated: November 3, 2026

Triethylamine → 5-Tert-butyl-2-methoxy-3-nitro-benzyl methanesulphonate

https://huagongshe.com/reaction/2360514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(5-Tert-butyl-2-methoxy-3-nitrophenyl)methanolHCID 58493934—
SolventDichloromethaneHCID 6344—
Product5-Tert-butyl-2-methoxy-3-nitro-benzyl methanesulphonateHCID 58493954—

Reaction Conditions

Temperature0 °C

Reaction Steps

3.43 g (5-tert-butyl-2-methoxy-3-nitro-phenyl)-methanol are dissolved in 30 ml dichloromethane, combined with 2.39 ml of triethylamine and cooled to 0° C. 1.2 g of methanesulphonic acid chloride are added dropwise and the mixture is stirred for 2 hours. Then it is diluted with dichloromethane and washed 3 times with water and once with saturated aqueous sodium chloride solution. After drying with magnesium sulphate the solvents are eliminated in vacuo and the product thus obtained is further reacted directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686022B2
Source datasetuspto-grants-2014_04
ORD IDord-e99786ebe4314e7fb79c507b25c96553
Source noteuspto-grants-2014_04