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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003853Generated: October 25, 2026

Methanol → Methyl 5-(tert-butyl)-4-hydroxy-2-methylbenzoate

https://huagongshe.com/reaction/1003853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant5-tert-Butyl-4-(2-methoxy-ethoxymethoxy)-2-methyl benzoic acidHCID 54066845—
ProductMethyl 5-(tert-butyl)-4-hydroxy-2-methylbenzoateHCID 10632819—

Reaction Steps

A solution of 5-tert-butyl-4-(2-methoxy-ethoxymethoxy)-2-methyl benzoic acid from Example AAA (20.9 g, 70.5 mmol), MeOH (150 mL), and H2SO4 (10 mL) was refluxed for 5 hours and stirred overnight at room temperature. The mixture was concentrated by half, diluted with H2O, and extracted with EtOAc. The combined extracts were washed with brine, dried (MgSO4), and concentrated to give the title compound. 1H NMR (CDCl3) δ 1.36 (s, 9 H), 2.48 (s, 3 H), 3.82 (s, 3 H), 6.48 (s, 1 H), 7.87 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046355
Source datasetuspto-grants-2000_04
ORD IDord-01368955834243c8a88831912aa0f809
Source noteuspto-grants-2000_04