Acetone → (4-tert-Butoxycarbonylamino-naphthalen-1-yloxy)-acetic Acid Ethyl Ester

Reaktionsgleichung

[Br:26][CH2:27][C:28](=[O:29])[O:30][CH2:31][CH3:32].[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([NH:7][c:8]1[cH:9][cH:10][c:11]([OH:18])[c:12]2[cH:13][cH:14][cH:15][cH:16][c:17]12)=[O:19].[C:20](=[O:21])([O-:22])[O-:23].[CH3:33][C:34](=[O:35])[CH3:36].[Cs+:24].[Cs+:25]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([NH:7][c:8]1[cH:9][cH:10][c:11]([O:18][CH2:27][C:28](=[O:29])[O:30][CH2:31][CH3:32])[c:12]2[cH:13][cH:14][cH:15][cH:16][c:17]12)=[O:19]

Komponenten

Edukt 5

HCID 180Acetone

HCID 7748Ethyl bromoacetate

HCID 19660Carbonate Ion

HCID 104967Cesium cation2×

HCID 10923237tert-Butyl (4-hydroxynaphthalen-1-yl)carbamate

Produkt 1

HCID 69037445(4-tert-Butoxycarbonylamino-naphthalen-1-yloxy)-acetic Acid Ethyl Ester

Quellen und Nachweise

ORD-Eintrag: ord-8ce36649bf284e549b002dbf1e720a0c
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

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