Chloride → HCID 178468531, compound

HRID 196998Notes

Reaction equation

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

Participants

Reactant 7

HCID 312Chloride

HCID 702Ethanol

HCID 813Potassium Cation4×

HCID 1003Dihydrogenphosphate

HCID 24749GlyTouCan:G09597LJ

HCID 3681305Hydrogen phosphate

HCID 12177975ethyl 5-methoxy-1-oxo-2,3-dihydro-1H-indene-2-carboxylate

Product 1

HCID 178468531HCID 178468531, compound

Sources & evidence

ORD record: ord-8ce66286c04841bb91f8b89c7fa015fc
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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