HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Trityl chloride → (s)-2-(Tritylamino)butan-1-ol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Trityl chloride | HCID 6456 | — |
| Edukt | Hexane | HCID 8058 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-Amino-1-butanol, (+)- | HCID 120084 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (s)-2-(Tritylamino)butan-1-ol | HCID 57433108 | — |
Reaktionsschritte
To a stirred solution of (S)-(+)-2-aminobutan-1-ol (10 g, 112.18 mmol) in dichloromethane (DCM, 250 ml) under an argon atmosphere at room temperature, was added diisopropylethylamine (DIEA, 19.4 ml, 112.18 mmol) followed by trityl chloride (31.2 g, 112.18 mmol). The reaction mixture was stirred at this temperature for 48 h, when TLC (hexane:ether:MeOH; 55:40:5) indicated that the reaction had gone to completion. The solvent was evaporated in vacuo and the residue taken up in ethyl acetate. The organic solution was washed with water (2×), dried over sodium sulphate. The solvent was removed to afford (S)-2-(trityl-amino)-butan-1-ol as a light yellow oil;
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09173938B2 |
| Quelldatensatz | uspto-grants-2015_11 |
| ORD ID | ord-35eb8d13938a451394d24414a3bbba55 |
| Quellennotiz | uspto-grants-2015_11 |