HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → chloromethyl (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Boc-L-Valine | HCID 83693 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Water | HCID 962 | — |
| Product | chloromethyl (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methylbutanoate | HCID 54112037 | — |
Reaction Steps
To a mixture of (S)-2-(t-butoxycarbonylamino)-3-methylbutanoic acid (28.6 g, 130 mmol) and NaHCO3 (44 g, 520 mmol) and Bu4NHSO4 (4.4 g, 13 mmol) in DCM (200 mL) and water (200 mL) was added chloromethyl sulfochloridate (26 g, 158 mmol) at 0° C. The mixture was stirred at room temperature for 24 hours, and then was extracted with DCM (3×150 mL). The combined organic layers were washed with water (2×300 mL), and the DCM layer was purified by flash column (petroleum ether:EA=15:1) to yield the title compound as a yellow solid (35 g). LC-MS: 266 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108934B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-63773046c64843d28ce9230623933470 |
| Source note | uspto-grants-2015_08 |