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Chloride → HCID 21888254, compound

HRID 311520
Notes
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Reaction equation

HRID 311520 reaction equation
[CH2:40]1[O:41][CH2:42][CH2:43][CH2:44]1.[CH3:11][CH2:12][N:13]([CH2:14][CH3:15])[CH2:16][CH3:17].[CH3:18][C:19]([CH3:20])([CH3:21])[C:22]([Cl:23])=[O:24].[CH3:1][CH:2]([CH2:3][CH2:4][C:5](=[O:6])[OH:7])[CH2:8][CH2:9][CH3:10].[CH3:27][CH:28]1[NH:29][C:30](=[O:39])[O:31][CH:32]1[c:33]1[cH:34][cH:35][cH:36][cH:37][cH:38]1.[Cl-:25].[Li+:26]>>[CH3:1][CH:2]([CH2:3][CH2:4][C:5](=[O:7])[N:29]1[CH:28]([CH3:27])[CH:32]([c:33]2[cH:34][cH:35][cH:36][cH:37][cH:38]2)[O:31][C:30]1=[O:39])[CH2:8][CH2:9][CH3:10]
ParticipantsSources & evidenceReaction notes

Participants

8

Reactant 7

HCID 312ChlorideHCID 8028TetrahydrofuranHCID 8471TriethylamineHCID 28486Lithium ionHCID 62493Pivaloyl chlorideHCID 2501744-Methyl-5-phenyl-1,3-oxazolidin-2-oneHCID 138003694-Methylheptanoic acid

Product 1

On this pageParticipantsSources & evidenceReaction notes
HCID 21888254HCID 21888254, compound

Sources & evidence

ORD record
ord-fdf24cf3e4814c0fa7232cbc4d1309ad
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI
10.1039/C8SC04228D

Reaction notes

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