Pyridine → 1-Acetoxy-5-chloro-2-methylsulfonylindane

Reaction equation

[CH3:22][C:23](=[O:24])[O:25][C:26](=[O:27])[CH3:28].[Cl:1][c:2]1[cH:3][c:4]2[c:8]([cH:9][cH:10]1)[CH:7]([OH:11])[CH:6]([S:12](=[O:13])(=[O:14])[CH3:15])[CH2:5]2.[Cl:29][CH2:30][Cl:31].[cH:16]1[cH:17][cH:18][n:19][cH:20][cH:21]1>>[Cl:1][c:2]1[cH:3][c:4]2[c:8]([cH:9][cH:10]1)[CH:7]([O:11][C:23]([CH3:22])=[O:24])[CH:6]([S:12](=[O:13])(=[O:14])[CH3:15])[CH2:5]2

Participants

Reactant 4

HCID 1049Pyridine

HCID 6344Dichloromethane

HCID 7918Acetic Anhydride

HCID 98347545-Chloro-2-methylsulfonylindan-1-ol

Product 1

HCID 99438231-Acetoxy-5-chloro-2-methylsulfonylindane

Sources & evidence

ORD record: ord-4906d8bd2a6743aab213a668dc9eae59
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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