HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361528Generated: October 30, 2026
o-Xylyl bromide → Methyl 3-hydroxy-5-{[(2-methylphenyl)methyl]oxy}benzoate
https://huagongshe.com/reaction/1361528
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | o-Xylyl bromide | HCID 6992 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 3,5-Dihydroxybenzoate | HCID 75076 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-hydroxy-5-{[(2-methylphenyl)methyl]oxy}benzoate | HCID 21074227 | 29.8% |
Reaction Steps
To a solution of methyl 3,5-dihydroxybenzoate (50 g, 0.30 mol) in DMF (500 ml) at 0° C. was added sodium hydride (10.8 g, 0.27 mol) portion wise. The reaction was allowed to warm to 15° C., and stirred for 20 minutes. The mixture was re-cooled to 0° C. and a solution of 2-methylbenzyl bromide (36 ml, 0.27 mol) in DMF (50 ml) was added over 30 minutes. The reaction was warmed to ambient temperature and concentrated in vacuo. The residual oil was partitioned between ethyl acetate (500 ml) and water (250 ml), and the ethyl acetate layer was separated, washed with water and evaporated. The residue was purified by column chromatograph on silica gel (gradient, 0-100% ethyl acetate in isohexane) to give the desired compound (21.9 g, 27%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880012B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-8fd60ed9337946ae96816980a4428be1 |
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| Source note | uspto-grants-2011_02 |
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