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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzenesulfonic acid hydrateHCID 12496995—
ReactantHCID 86626188HCID 86626188—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductHCID 86626187HCID 8662618794%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754737B2
Source datasetuspto-grants-2010_07
ORD IDord-f552265ae26940c6931912258ef1c48c
Source noteuspto-grants-2010_07