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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061955Generated: November 1, 2026

Methanol → 1,3-Di-tert-butylbenzene

https://huagongshe.com/reaction/2061955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium formateHCID 2723923—
ReactantLithium acetateHCID 3474584—
Reactant2,4-Di-tert-butylphenyl methanesulfonateHCID 44542716—
CatalystHCID 178418390HCID 178418390—
SolventWaterHCID 962—
Product1,3-Di-tert-butylbenzeneHCID 13681076.4%

Reaction Steps

In a nitrogen atmosphere under normal pressure, 2,4-di-tert-butylphenyl methanesulfonate (30 g, 0.11 mols), ammonium formate (8.0 g, 0.13 mols), lithium acetate (8.4 g, 0.13 mols) and methanol (45 g) were mixed at 25° C., and with stirring, 10 mass % Pd/carbon (50 mass % water-containing product) (1.2 g) (as metal palladium; 0.2 mass % relative to 2,4-di-tert-butylphenyl methanesulfonate) as supported by a carbon carrier having a specific surface area of 780 m2/g (by BET method) was put into it. With stirring, the reaction liquid was reacted at the same temperature for 4 hours. Water (10 mL) was added to the reaction liquid and Pd-carbon was separated through filtration, then heptane (30 g) was added to the filtrate. The organic layer obtained after extraction was concentrated under reduced pressure to give crude 1,3-di-tert-butylbenzene (16 g, yield 81% by mass). The result is shown in Table II-3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283508B2
Source datasetuspto-grants-2012_10
ORD IDord-516df89a13fa431da3235f401849ab7a
Source noteuspto-grants-2012_10