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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061956Generated: October 25, 2026

Methanol → 1,3-Di-tert-butylbenzene

https://huagongshe.com/reaction/2061956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantLithium formateHCID 23680280—
Reactant2,4-Di-tert-butylphenyl methanesulfonateHCID 44542716—
CatalystHCID 178418390HCID 178418390—
SolventWaterHCID 962—
Product1,3-Di-tert-butylbenzeneHCID 13681075.1%

Reaction Steps

Using the thus-obtained, regenerated Pd/carbon (10 g), the same reaction as in Example II-1 was carried out in a nitrogen atmosphere under normal pressure at 25° C., in which, however, 2,4-di-tert-butylphenyl methanesulfonate (100 g, 0.35 mols), lithium formate (37 g, 0.70 mols) and methanol (600 g) were used. Water (20 mL) was added to the reaction liquid and Pd/carbon was collected through filtration, and heptane (100 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 (50 g, yield 75% by mass).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283508B2
Source datasetuspto-grants-2012_10
ORD IDord-6c0860746d36495db6d05fdabf44a465
Source noteuspto-grants-2012_10