HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935759Generated: November 1, 2026
Hydroxyphenylacetic acid → Tert-butyl 2-(4-hydroxyphenyl)acetate
https://huagongshe.com/reaction/1935759
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyphenylacetic acid | HCID 127 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Tert-butyl 2-(4-hydroxyphenyl)acetate | HCID 15932404 | 56% |
Reaction Steps
A stirred suspension of 4-hydroxy-phenyl acetic acid (0.152 g, 1 mmol) in anhydrous toluene (5 mL) was heated at 80° C. and N,N-dimethyl formamide-di-ti-butyl acetal (1 mL, 4.17mmol) was added when the solution became homogenous. After 0.5 h, the reaction mixture was cooled to ambient temperature and the volatiles were distilled off in vacuo. The residue was diluted with water and extracted with diethyl ether (×2). The combined organic extract was dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to afford an oil which was subjected to flash column chromatography over silica gel (230-400 mesh) using 16% ethyl acetate in hexane as the eluent to afford the title compound as a solid (0.11 g, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06387892B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-5ced73dcd79c4c9bbd6145c7fe67d1b8 |
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| Source note | uspto-grants-2002_05 |
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