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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182791Generated: November 1, 2026

Dimethyl Sulfate → Methyl 4-benzyloxy-5-isopropyl-2-methoxybenzoate

https://huagongshe.com/reaction/1182791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-benzyloxy-2-hydroxy-5-isopropylbenzoateHCID 58236452—
SolventAcetonitrileHCID 6342—
ProductMethyl 4-benzyloxy-5-isopropyl-2-methoxybenzoateHCID 5823647295%

Reaction Steps

Anhydrous potassium carbonate (450 mg, 3.26 mmol) and dimethyl sulphate (0.25 ml, 2.64 mmol) were added to a suspension of methyl 4-benzyloxy-2-hydroxy-5-isopropylbenzoate (650 mg, 2.17 mmol) in acetonitrile (20 ml) and the mixture was stirred and held at reflux for 16 hours. Upon cooling to room temperature the solvent was removed in vacuo and the residue acidified by the addition of 2M hydrochloric acid (20 ml). The organic material was extracted with ethyl acetate (2×30 ml) and the combined organic extracts were evaporated in vacuo to afford methyl 4-benzyloxy-5-isopropyl-2-methoxybenzoate (644 mg, 95%) as a pale yellow solid. 1H NMR (DMSO-d6) 7.56 (1H, s), 7.50 (2H, d), 7.43 (2H, t), 7.37 (1H, t), 6.80 (1H, s), 5.26 (2H, s), 3.83 (3H, s), 3.75 (3H, s), 3.19 (1H, m), 1.17 (6H, d). MS: [M+H]+ 315.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664218B2
Source datasetuspto-grants-2014_03
ORD IDord-d451771b254f477ba0319c26ca67db32
Source noteuspto-grants-2014_03