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2,6-Lutidine → p-Nitrobenzyl 2-(4-ethylthio-2-oxo-1-azetidinyl)-2-chloroacetate

HRID 91697
Notes
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Reaction equation

HRID 91697 reaction equation
[CH2:1]([CH3:2])[S:3][CH:4]1[CH2:5][C:6](=[O:23])[N:7]1[CH:8]([C:9](=[O:10])[O:11][CH2:12][c:13]1[cH:14][cH:15][c:16]([N+:19](=[O:20])[O-:21])[cH:17][cH:18]1)[OH:22].[CH3:24][c:25]1[n:26][c:27]([CH3:28])[cH:29][cH:30][cH:31]1.[O:36]1[CH2:37][CH2:38][CH2:39][CH2:40]1.[S:32]([Cl:33])([Cl:34])=[O:35]>>[CH2:1]([CH3:2])[S:3][CH:4]1[CH2:5][C:6](=[O:23])[N:7]1[CH:8]([C:9](=[O:10])[O:11][CH2:12][c:13]1[cH:14][cH:15][c:16]([N+:19](=[O:20])[O-:21])[cH:17][cH:18]1)[Cl:34]
ParticipantsSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 79372,6-LutidineHCID 8028TetrahydrofuranHCID 24386Thionyl ChlorideHCID 14050377p-Nitrobenzyl 2-(4-ethylthio-2-oxo-1-azetidinyl)-2-hydroxyacetate

Product 1

HCID 14050378p-Nitrobenzyl 2-(4-ethylthio-2-oxo-1-azetidinyl)-2-chloroacetate

Sources & evidence

ORD record
ord-f06dd9a01530467eb8732d294253fabb
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes