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Ammonium → HCID 22032377, compound

HRID 1546328
Notes
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Reaction equation

HRID 1546328 reaction equation
[Br:1][c:2]1[s:3][c:4]([S:7][CH3:8])[cH:5][cH:6]1.[CH2:9]([Li:10])[CH2:11][CH2:12][CH3:13].[CH3:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41].[CH:14](=[O:15])[CH:16]1[CH2:17][CH2:18][N:19]([C:22](=[O:23])[O:24][C:25]([CH3:26])([CH3:27])[CH3:28])[CH2:20][CH2:21]1.[Cl-:29].[NH4+:30].[O:31]1[CH2:32][CH2:33][CH2:34][CH2:35]1.[OH2:42]>>[c:2]1([CH:14]([OH:15])[CH:16]2[CH2:17][CH2:18][N:19]([C:22](=[O:23])[O:24][C:25]([CH3:26])([CH3:27])[CH3:28])[CH2:20][CH2:21]2)[s:3][c:4]([S:7][CH3:8])[cH:5][cH:6]1
ParticipantsSources & evidenceReaction notes

Participants

9

Reactant 8

HCID 223AmmoniumHCID 312ChlorideHCID 962WaterHCID 8028TetrahydrofuranHCID 8058HexaneHCID 1514430tert-Butyl 4-formylpiperidine-1-carboxylateHCID 220320322-Bromo-5-(methylthio)thiophene
On this pageParticipantsSources & evidenceReaction notes
HCID 178418339
Butyllithium

Product 1

HCID 22032377HCID 22032377, compound

Sources & evidence

ORD record
ord-6451cf6dfd3f44e3a99d2f3540ca5c2d
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI
10.1039/C8SC04228D

Reaction notes

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