HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348301Generated: October 30, 2026
4-tert-Butylphenol → Ethyl 2-(4-tert-butylphenoxy)propanoate
https://huagongshe.com/reaction/348301
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-bromopropionate | HCID 79040 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-(4-tert-butylphenoxy)propanoate | HCID 3023318 | 100% |
Reaction Steps
4-tert-butylphenol (7.52 g, 50 mmol) in anhydrous DMF (40 mL) was added dropwise to NaH (2.2 g, 55 mmol, 60% w/w in mineral oil) at 0° C. under an atmosphere of nitrogen. After five min, ethyl 2-bromopropionate (6.49 mL, 50 mmol, d=1.394) was added rapidly dropwise and the resultant mixture was allowed to stir for 18 h, gradually warming to ambient temperature. The reaction mixture was diluted with ethyl acetate (300 mL) and extracted twice with water and once with brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to produce a colorless oil (12.5 g, 100%) 1H NMR (300 MHz, CDCl3): δ 7.28 (d, 2H, J=5.5), 6.80 (d, 2H, J=5.5), 4.70 (q, 1H, J=6.6), 4.22 (q, 2H, J=7.1), 1.59 (d, 3H, J=6.6), 1.28 (s, 9H), 1.25 (t, 3H, J=7.1). MS [EI+] 251 (M+H)+, 268 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176224B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-b3ef37844ef2488086f61b09b05df4e6 |
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| Source note | uspto-grants-2007_02 |
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