HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488267Generated: October 28, 2026
Benzyl Bromide → 3-(Octadecyloxy)-5-(phenylmethoxy)benzoic acid methyl ester
https://huagongshe.com/reaction/488267
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Hydroxy-5-(octadecyloxy)benzoic acid methyl ester | HCID 15233478 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(Octadecyloxy)-5-(phenylmethoxy)benzoic acid methyl ester | HCID 54033513 | 89.3% |
Reaction Steps
A mixture of 3.0 g (7.1 mmol) of 3-hydroxy-5-(octadecyloxy) benzoic acid methyl ester, 0.93 ml (7.85 mmol) of benzyl bromide and 2.0 g (14.5 mmol) of potassium carbonate in 50 ml of DMF was stirred at 85° for 50 hours. The solvent was removed at reduced pressure and the residue was extracted with methylene chloride. The extract was concentrated and recrystallized from methylene chloride-methanol to give 3.24 g (89% yield, mp 62°-64°) of 3-(octadecyloxy)-5-(phenylmethoxy)benzoic acid methyl ester. A solution of 3.24 g (6.3 mmol) of 3-(octadecyloxy)-5-(phenylmethoxy) benzoic acid methyl ester and 3 ml (18 mmol) of 6N NaOH in 100 ml of methanol and 25 ml of dioxane was stirred at reflux for 3.5 hours. The solvents were removed at reduced pressure and the residue was acidified and extracted with ethyl acetate. The dried extract was concentrated to a solid which was recrystallized from methylene chloride-hexane to give 2.77 g (88% yield, mp 101°-103°) of 3-(octadecyloxy)-5-(phenylmethoxy)benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05298652 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-56fc58b114df49209de6afe9dcbc0c4a |
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| Source note | uspto-grants-1994_03 |
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