Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl chloroformate | HCID 6586 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Boc-DTrp-OBzl | HCID 10739405 | — |
| Katalysator | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Boc-DTrp(COOMe)-OBzl | HCID 10813513 | 123,8% |
Reaktionsschritte
To a solution of Boc-DTrp-OBzl(1 g) in dichloromethane(8 ml) was added Bu4NHSO4 (8.62 mg) and pulverized NaOH(253 mg) under ice cooling. To the resulting suspension was added dropwise a solution of methyl chloroformate(599 mg) in dichloromethane(6 ml) under ice cooling over a period of 30 min. The reaction mixture was stirred under ice cooling for 30 min and at room temperature for 12 h, diluted with dichloromethane, washed successively with water, 5% KHSO., saturated NaHCO3 and saturated NaCl, dried over MgSO4, and filtered. The filtrate was concentrated under reduced pressure to give Boc-DTrp(COOCH3)-OBzl(1.42 g) as a colorless solid. The solid was hydrogenolized over a catalytic amount of 10% Pd/C in methanol under an atmosphere of hydrogen(under atmospheric pressure) to give Boc-DTrp(COOCH3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05114918 |
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| Quelldatensatz | uspto-grants-1992_05 |
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| ORD ID | ord-dbdcf614e9dd4c529c992f2a6ada03a6 |
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| Quellennotiz | uspto-grants-1992_05 |
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