HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(Benzyloxycarbonylamino)-3-(1-methylcyclohexyl)propyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Benzyl 1-hydroxy-3-(1-methylcyclohexyl)propan-2-ylcarbamate | HCID 59201634 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Benzyloxycarbonylamino)-3-(1-methylcyclohexyl)propyl methanesulfonate | HCID 86639448 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A mixture of 0.3607 g (1.18 mmol) of benzyl 1-hydroxy-3-(1-methylcyclohexyl)propan-2-ylcarbamate, 0.4 mL (2.87 mmol, 2.43 equiv) of triethylamine, 0.1 mL (1.29 mmol, 1.09 equiv) of methanesulfonyl chloride in CH2Cl2 (10 mL) was stirred at 0° C. for 1.5 h. The reaction mixture was quenched with ice water, extracted with CH2Cl2, washed with aqueous NaHCO3, and dried over Na2SO4. After the solvent was removed in vacuo, the crude 2-(benzyloxycarbonylamino)-3-(1-methylcyclohexyl)propyl methanesulfonate was used directly in the next step without further purification. MS ESI +ve m/z 406 (M+Na).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08487108B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-955a3d1e77ea42498895707e1b154213 |
| Source note | uspto-grants-2013_07 |