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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571575Generated: October 31, 2026

Butylated Hydroxyanisole → 2-Tert-butyl-4-methoxyphenyl methanesulfonate

https://huagongshe.com/reaction/571575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButylated HydroxyanisoleHCID 8456—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
SolventDimethyl CarbonateHCID 12021—
Product2-Tert-butyl-4-methoxyphenyl methanesulfonateHCID 8666828576%

Reaction Conditions

Temperature25 °C

Reaction Steps

15.0 g (83.2 mmol) of 4-hydroxy-3-tert-butylanisole and 10.5 g (104 mmol) of triethylamine were dissolved in 250 ml of dimethyl carbonate (solvent), and 11.9 g (104 mmol) of methanesulfonyl chloride was dropwise added thereto, taking 25 minutes and controlling the inner temperature at 5° C. or lower. After the addition, this was stirred at 25° C. for 1.5 hours, the reaction mixture was poured into an aqueous saturated sodium bicarbonate solution, the aqueous layer was separated, the organic layer was washed twice with water, and then the organic layer was separated and concentrated. The concentrate was purified through distillation (139° C./32 pa) to give 16.3 g of 2-tert-butyl-4-methoxyphenyl methanesulfonate (yield, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029024B2
Source datasetuspto-grants-2015_05
ORD IDord-e6cb5f084f1e46d0a94f4f047535c050
Source noteuspto-grants-2015_05