Ammonium → HCID 178504415, compound

HRID 1220115Notes

Reaction equation

[C:15]([CH3:16])([CH3:17])([CH3:18])[O:19][C:20](=[O:21])[N:22]1[C:23]([CH2:31][OH:32])([O:33][SiH:34]([CH3:35])[CH3:36])[CH2:24][CH:25]([C:27]([CH3:28])([CH3:29])[CH3:30])[CH2:26]1.[CH2:39]([Cl:40])[Cl:41].[CH:1]([N:2]([CH2:3][CH3:4])[CH:5]([CH3:6])[CH3:7])([CH3:8])[CH3:9].[Cl-:37].[NH4+:38].[S:10](=[O:11])(=[O:12])([CH3:13])[Cl:14]>>[S:10](=[O:11])(=[O:12])([CH3:13])[O:32][CH2:31][C:23]1([O:33][SiH:34]([CH3:35])[CH3:36])[N:22]([C:20]([O:19][C:15]([CH3:16])([CH3:17])[CH3:18])=[O:21])[CH2:26][CH:25]([C:27]([CH3:28])([CH3:29])[CH3:30])[CH2:24]1

Participants

Reactant 6

HCID 223Ammonium

HCID 312Chloride

HCID 6344Dichloromethane

HCID 31297Methanesulfonyl chloride

HCID 81531Diisopropylethylamine

HCID 173364780Tert-butyl 4-tert-butyl-2-dimethylsilyloxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate

Product 1

HCID 178504415HCID 178504415, compound

Sources & evidence

ORD record: ord-9f0d8861549b40b693ed656a3344a6e6
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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