HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586768Generated: November 1, 2026
Water → tert-Butyl 3-(4'-Hydroxyphenyl)mercaptopivaloate
https://huagongshe.com/reaction/1586768
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Mercaptophenol | HCID 240147 | — |
| Reactant | Tert-butyl 3-chloropivaloate | HCID 22590969 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl 3-(4'-Hydroxyphenyl)mercaptopivaloate | HCID 21695402 | 60% |
Reaction Steps
To a slurry of 4-hydroxythiophenol (259.4 g, 2.06 mol) and potassium carbonate (284.2 g, 2.06 mol) in 500 mL of DMF at 0° C. was added tert-butyl 3-chloropivaloate (373.8 g, 1.94 mol) dropwise over 2 hours. After stirring to room temperature overnight, the reaction was heated to 110° C. for 3 hours. The reaction was allowed to cool for room temperature and water and ether were added. The layers were separated and the organic layer washed with water and 5% NaOH, dried over MgSO4 and concentrated. The resulting oil was recrystallized from 1:3 CH2Cl2 /pet. ether to afford 328.0 g (60%) of the desired product. mp 100°-100.5° C.; 1H NMR (CDCl3) δ1.22 (s,6H), 1.44 (s,9H), 3.07 (s,2H), 5.42 (br s,1H,--OH), 6.77 (d,2H,J=8.7 Hz); 13C NMR (CDCl3) δ 24.62, 27.73, 44.58, 46.86, 81.00, 116.2, 127.7, 133.5, 155.4, 176.7; IR (KBr, film) 3362, 2971, 1720, 1693, 1600, 1583, 1495, 1472, 1366, 1320, 1223, 1150(s), 835, 817 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05216022 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-a9bcf706e32c4a55bdeb718fa017de7b |
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| Source note | uspto-grants-1993_06 |
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