HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → HCID 28165234, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | BOC-D-alanine | HCID 637606 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 28165234 | HCID 28165234 | 76% |
Reaction Steps
To a solution of (R)-2-tert-Butoxycarbonylamino-propionic acid (1.78 g, 9.43 mmol) in DCM (7.85 mL) was added portion wise DCC (2.14 g, 10.37 mmol) cooled in an ice bath. After stirring at room temperature for 30 min, dimethylamine (2 M in THF) (6.13 mL, 12.25 mmol) was added. The resulting solution was stirred overnight (18 h) until reaction was completed. The reaction mixture was filtered through silica gel and eluted with Ethyl acetate. Then the filtrate was evaporated off. The solvent was removed to yield (1.71 g, 7.12 mmol, 76% yield, 90% purity) ((R)-1-Dimethylcarbamoyl-ethyl)-carbamic acid tert-butyl ester as a yellow oil. The product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056843B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-11e319770c644f299b9baba76b30b38f |
| Source note | uspto-grants-2015_06 |