HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040802Generated: October 29, 2026
Dimethylformamide → 3-Ethyl-4-hydroxy-5-methyl-benzoic acid benzyl ester
https://huagongshe.com/reaction/2040802
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3-Ethyl-4-hydroxy-5-methyl-benzoic acid | HCID 59234777 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Ethyl-4-hydroxy-5-methyl-benzoic acid benzyl ester | HCID 68550259 | 90% |
Reaction Steps
To a solution of 3-ethyl-4-hydroxy-5-methyl-benzoic acid (80.3 g, 0.446 mol) is DMF (500 mL), KHCO3 (53.5 g, 0.535 mol) followed by benzylbromide (114.3 g, 0.668 mol) is added. The mixture is stirred at 50° C. for 18 h before it is cooled to rt, diluted with water (250 mL), and extracted with TBME (2×250 mL). The org. extracts are washed with water, and then concentrated. The crude product is purified by CC on silica gel eluting with heptane:EA 19:1 to 9:1 to give 3-ethyl-4-hydroxy-5-methyl-benzoic acid benzyl ester (108.5 g) as a beige solid; 1H NMR (CDCl3): δ 1.28 (t, J=7.5 Hz, 3 H), 2.30 (s, 3 H), 2.68 (q, J=7.8 Hz, 2 H), 5.24 (s, 1 H), 5.37 (s, 2 H), 7.33-7.45 (m, 3 H), 7.45-7.50 (m, 2 H), 7.77 (s, 1 H), 7.79 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580824B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-edce014358614799a18e31045f5fa7fe |
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| Source note | uspto-grants-2013_11 |
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