HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389949Generated: October 29, 2026
Dimethyl Sulfate → Methyl 4-benzyloxy-5-isopropyl-2-methoxybenzoate
https://huagongshe.com/reaction/389949
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 4-benzyloxy-2-hydroxy-5-isopropylbenzoate | HCID 58236452 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 4-benzyloxy-5-isopropyl-2-methoxybenzoate | HCID 58236472 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383619B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-952ad342f3a14003a48f93b19f045e37 |
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| Source note | uspto-grants-2013_02 |
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