Bromide ion → Methyl 3-amino-5-bromothiophene-2-carboxylate

HRID 161356

Reaktionsgleichung

[Br-:11].[Br-:12].[Br-:13].[CH2:49]([Cl:50])[Cl:51].[CH3:1][O:2][C:3](=[O:4])[c:5]1[s:6][cH:7][cH:8][c:9]1[NH2:10].[CH3:52][OH:53].[Ca+2:44].[O-:45][C:46](=[O:47])[O-:48].[c:14]1([N+:15]([CH3:16])([CH3:17])[CH3:18])[cH:19][cH:20][cH:21][cH:22][cH:23]1.[c:24]1([N+:25]([CH3:26])([CH3:27])[CH3:28])[cH:29][cH:30][cH:31][cH:32][cH:33]1.[c:34]1([N+:35]([CH3:36])([CH3:37])[CH3:38])[cH:39][cH:40][cH:41][cH:42][cH:43]1>>[CH3:1][O:2][C:3](=[O:4])[c:5]1[s:6][c:7]([Br:11])[cH:8][c:9]1[NH2:10]

Komponenten

Edukt 7

HCID 259Bromide ion3×

HCID 271Calcium Cation

HCID 887Methanol

HCID 6344Dichloromethane

HCID 15914Phenyltrimethylammonium3×

HCID 19660Carbonate Ion

HCID 89652Methyl 3-amino-2-thiophenecarboxylate

Produkt 1

HCID 20158931Methyl 3-amino-5-bromothiophene-2-carboxylate

Quellen und Nachweise

ORD-Eintrag: ord-e85b7d44e4404263944fa595caf030eb
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D

Verknüpfte Notizen

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