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2,6-Lutidine → p-Nitrobenzyl 2-chloro-2-(4-methylthio-2-azetidinon-1-yl)acetate

HRID 666993
Notes
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Reaction equation

HRID 666993 reaction equation
[CH3:40][CH2:41][O:42][C:43](=[O:44])[CH3:45].[O:35]1[CH2:36][CH2:37][CH2:38][CH2:39]1.[OH:13][CH:14]([C:15](=[O:16])[O:17][CH2:18][c:19]1[cH:20][cH:21][c:22]([N+:25](=[O:26])[O-:27])[cH:23][cH:24]1)[N:28]1[C:29](=[O:34])[CH2:30][CH:31]1[S:32][CH3:33].[S:9]([Cl:10])([Cl:11])=[O:12].[n:1]1[c:2]([CH3:3])[cH:4][cH:5][cH:6][c:7]1[CH3:8]>>[Cl:11][CH:14]([C:15](=[O:16])[O:17][CH2:18][c:19]1[cH:20][cH:21][c:22]([N+:25](=[O:26])[O-:27])[cH:23][cH:24]1)[N:28]1[C:29](=[O:34])[CH2:30][CH:31]1[S:32][CH3:33]
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 79372,6-LutidineHCID 8028TetrahydrofuranHCID 8857Ethyl AcetateHCID 24386Thionyl ChlorideHCID 20220832p-Nitrobenzyl 2-hydroxy-2-(4-methylthio-2-azetidinon-1-yl)acetate

Product 1

HCID 20220789p-Nitrobenzyl 2-chloro-2-(4-methylthio-2-azetidinon-1-yl)acetate

Sources & evidence

ORD record
ord-71454f0cf5464d6cb4243aab29d11246
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes