HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355482Generated: October 31, 2026
p-Toluenesulfonic acid → HCID 57544576, compound
https://huagongshe.com/reaction/2355482
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 57544970 | HCID 57544970 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57544576 | HCID 57544576 | 90.4% |
Reaction Steps
To a solution of (S)-tert-butyl 4-(2-methoxy-2-methylpropyl)-2,2-dimethyloxazolidine-3-carboxylate (1.2 g, 3.40 mmol) in MeOH (5 mL) at rt, there was added 4-methylbenzenesulfonic acid (0.65 g, 3.40 mmol). The resulting solution was stirred until no starting material remained (˜1 h). Solvent was removed under vacuum, and the residue was redissolved in acetone (3 mL) and H2O (1 mL). Excess K2CO3 was added to keep the solution basic, followed by (Boc)2O. The mixture was stirred for 20 min, acetone was removed under vacuum, and the aqueous solution was extracted with CH2Cl2 (4×5 mL). After concentration, the residue was purified by flash column chromatography to give (S)-tert-butyl 1-hydroxy-4-methoxy-4-methylpentan-2-ylcarbamate (0.76 g, 78%, 2 steps). 1H NMR (400 MHz, CDCl3): 5.38 (br, 1H), 3.78 (m, 1H), 3.66 (m, 1H), 3.56 (m, 1H), 3.20 (s, 3H), 1.66 (m, 2H), 1.62 (br, 1H), 1.44 (s, 9H), 1.20 (s, 6H); MS m/z 248 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754737B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-a907e2012d544ca4a546f0c9ee1aa1d5 |
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| Source note | uspto-grants-2010_07 |
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