HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453409Generated: October 30, 2026
Benzyl Bromide → 4-Benzyloxy-2-ethyl-3-methylbenzoic acid
https://huagongshe.com/reaction/453409
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Ethyl-4-hydroxy-3-methylbenzoic acid | HCID 22717373 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Benzyloxy-2-ethyl-3-methylbenzoic acid | HCID 66818581 | — |
Reaction Steps
2.10 g of 2-ethyl-4-hydroxy-3-methylbenzoic acid (E1) are dissolved in 50 ml of acetone. 3.30 ml of benzyl bromide and 5.10 g of K2CO3 are subsequently added. The reaction suspension is heated under reflux for 18 h overnight, subsequently filtered off with suction, and the filtrate obtained is evaporated to dryness in vacuo. The residue is dissolved in 40 ml of ethanol, and 40 ml of 2.0 N NaOH solution are added. The mixture is then heated under reflux for 3 h. The clear solution is diluted with 150 ml of water and adjusted to pH 1 using 20% hydrochloric acid. After stirring for 30 min, the precipitate formed is filtered off with suction, rinsed with water and dried at 90° C. in vacuo overnight, giving 2.45 g of the title compound as a beige, amorphous solid having a melting point of 169° C.; MS: 270.0 (M+); TLC: Rf=0.36 (cyclohexane/ethyl acetate 2:1 parts by volume).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492440B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-7c7295df93174aa9aa0c3f9b5fa44091 |
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| Source note | uspto-grants-2013_07 |
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