HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,2-Trifluoroethanol → Methyl 3-(butylamino)butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Methyl 3-aminocrotonate | HCID 643918 | — |
| Reactant | Methyl 3-(n-butylamino)crotonate | HCID 12526222 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Product | Methyl 3-(butylamino)butanoate | HCID 22234711 | 10.6% |
Reaction Steps
The reaction was carried out in a manner similar to that in Example 9, except that 26.2 mg (0.0292 mmol) of Ru(OCOCH3)2((S)-tol-binap), 500 mg (2.92 mmol) of methyl 3-(n-butylamino)crotonate and 2.5 ml of 10% hydrogen chloride-methanol solution were used instead of 78.0 mg (0.0869 mmol) of Ru(OCOCH3)2((S)-tol-binap), 1.00 g (8.69 mmol) of methyl 3-aminocrotonate and 5 ml of 2,2,2-trifluoroethanol, respectively, and except that the reaction was carried out for 16 hours instead of 15 hours, and the reaction mixture was treated as in Example 9 to give methyl 3-(n-butylamino)butanoate in a yield of 10.6%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07015348B2 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-d27c56983c024d70bf1c413092ec5f44 |
| Source note | uspto-grants-2006_03 |