HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355344Generated: November 2, 2026
2-Methylbenzenesulfonic acid hydrate → HCID 86626187, compound
https://huagongshe.com/reaction/2355344
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylbenzenesulfonic acid hydrate | HCID 12496995 | — |
| Reactant | HCID 86626188 | HCID 86626188 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86626187 | HCID 86626187 | 94% |
Reaction Steps
A solution of toluenesulfonic acid monohydrate (10 mg, 0.053 mmol) in absolute ethanol (1 mL) was added to a solution of 2-(trimethylsilyl)ethyl (S)-3-cyclohexyl-2-((tert-butyl-carbamoyl)methylamino)propylcarbamate (21.3 mg, 0.51 mmol) in Et2O (10 mL). This solution was placed in a flask on a rotary evaporator and the Et2O was removed at ambient temp. The flask was then lowered into a water bath (60° C.) and selective removal of the Boc group proceeded concurrently with removal of the solvent. The reaction was complete within 2 h. This material was taken up in CH2Cl2 (20 mL) and 1N aq NaOH (10 mL) and extracted with CH2Cl2 (2×10 mL). The combined organic layers were washed with brine (2×5 mL), dried over Na2SO4, decanted, and stripped to afford 2-(trimethylsilyl)ethyl (S)-3-cyclohexyl-2-(methylamino)propylcarbamate (15.0 mg, 94%) as a clear film. MS ESI+ve m/z 315 (M+1).
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-f552265ae26940c6931912258ef1c48c |
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| Source note | uspto-grants-2010_07 |
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