Chloride → HCID 178504083, compound

HRID 201357Notes

Reaction equation

[C:14]([O:15][CH:18]1[CH:19]([CH:23]([CH3:24])[O:25][Si:26]([CH3:27])([CH3:28])[C:29]([CH3:30])([CH3:31])[CH3:32])[C:20](=[O:22])[NH:21]1)(=[O:16])[CH3:17].[C:8]([CH2:9][CH3:10])(=[S:11])[S:12][CH3:13].[CH3:1][CH2:2][N:3]([CH2:4][CH3:5])[CH2:6][CH3:7].[CH3:34][C:35]#[N:36].[Cl-:37].[Cl-:39].[Cl:40][CH2:41][Cl:42].[ClH:33].[Zn+2:38]>>[C:8]([CH:9]([CH3:10])[CH:18]1[CH:19]([CH:23]([CH3:24])[O:25][Si:26]([CH3:27])([CH3:28])[C:29]([CH3:30])([CH3:31])[CH3:32])[C:20](=[O:22])[NH:21]1)(=[S:11])[S:12][CH3:13]

Participants

Reactant 8

HCID 312Chloride2×

HCID 313Hydrochloric Acid

HCID 6342Acetonitrile

HCID 6344Dichloromethane

HCID 8471Triethylamine

HCID 32051Zinc(2+)

HCID 223580Methyl propanedithioate

HCID 4305700(2R,3S)-3-((R)-1-((tert-Butyldimethylsilyl)oxy)ethyl)-4-oxoazetidin-2-yl acetate

Product 1

HCID 178504083HCID 178504083, compound

Sources & evidence

ORD record: ord-779848ad0eee4dc9b8137a6fd7c84d0c
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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