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Bromide ion → 1-(1-(Naphthalen-1-ylsulfonyl)piperidin-4-yl)cyclopropanol

HRID 167623
Notes
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Reaction equation

HRID 167623 reaction equation
[Br-:1].[CH2:2]([CH3:3])[Mg+:4].[CH3:33][CH:34]([CH3:35])[O-:36].[CH3:37][CH:38]([CH3:39])[O-:40].[CH3:41][CH:42]([CH3:43])[O-:44].[CH3:45][Ti+3:46].[O:28]1[CH2:29][CH2:30][CH2:31][CH2:32]1.[c:5]1([S:15](=[O:16])(=[O:17])[N:18]2[CH2:19][CH2:20][CH:21]([C:24](=[O:25])[O:26][CH3:27])[CH2:22][CH2:23]2)[cH:6][cH:7][cH:8][c:9]2[cH:10][cH:11][cH:12][cH:13][c:14]12>>[CH2:2]1[CH2:3][C:24]1([CH:21]1[CH2:20][CH2:19][N:18]([S:15]([c:5]2[cH:6][cH:7][cH:8][c:9]3[cH:10][cH:11][cH:12][cH:13][c:14]23)(=[O:16])=[O:17])[CH2:23][CH2:22]1)[OH:25]
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 259Bromide ionHCID 8028TetrahydrofuranHCID 3260420Isopropanolate3×HCID 11950392Methyl 1-(naphthalen-1-ylsulfonyl)piperidine-4-carboxylateHCID 178461628HCID 178461628, compoundHCID 178477789HCID 178477789, compound

Product 1

HCID 11950394
1-(1-(Naphthalen-1-ylsulfonyl)piperidin-4-yl)cyclopropanol

Sources & evidence

ORD record
ord-e8270595f2ea40ff9a2f91343159c8d4
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes