HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexachloroethane → METHYL N-BOC-3-CHLORO-L-ALANINATE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexachloroethane | HCID 6214 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-Boc-L-serine methyl ester | HCID 7019177 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | HCID 87695156 | HCID 87695156 | — |
| Product | METHYL N-BOC-3-CHLORO-L-ALANINATE | HCID 12182794 | 61.4% |
Reaction Steps
A solution of triphenylphosphine (4.55 g, 17.4 mmol) and hexachloroethane (3.9 g, 16.5 mmol) in 1,2-dichloroethane (18 mL) prepared at 0° C. was added via cannula into a flask containing a solution of methyl N-(tert-butoxycarbonyl)-L-serinate (3.2 g, 14.6 mmol) in 1,2-dichloroethane DCE (40 mL), kept at 0° C. under N2 atmosphere. After the addition was completed, the reaction mixture was further stirred at room temperature for 2 h, diluted with DCM, washed with sat NaHCO3, dried over MgSO4, filtered and concentrated. Purification made through chromatographic column of silicagel eluted with 10% to 50% EtOAc in hexane for 30 min, to afford 2.13 g (61% yield) of title compound as white crystals. MS: m/z=260.0 (MNa+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187415B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-632dce4151594184ab5a458779f8e933 |
| Source note | uspto-grants-2015_11 |