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Tetrahydrofuran → HCID 178423892, compound

HRID 2320252
Notes
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Reaction equation

HRID 2320252 reaction equation
[CH3:32][CH2:33][CH2:34][CH2:35][N+:36]([CH2:37][CH2:38][CH2:39][CH3:40])([CH2:41][CH2:42][CH2:43][CH3:44])[CH2:45][CH2:46][CH2:47][CH3:48].[F-:31].[O:49]1[CH2:50][CH2:51][CH2:52][CH2:53]1.[c:1]1([CH3:2])[cH:3][cH:4][c:5]([S:6](=[O:7])(=[O:8])[n:10]2[n:11][c:12]([O:22][CH2:23][c:24]3[cH:25][cH:26][cH:27][cH:28][cH:29]3)[c:13](-[c:15]3[cH:16][cH:17][c:18]([CH3:21])[cH:19][cH:20]3)[cH:14]2)[cH:9][cH:30]1>>[nH:10]1[n:11][c:12]([O:22][CH2:23][c:24]2[cH:25][cH:26][cH:27][cH:28][cH:29]2)[c:13](-[c:15]2[cH:16][cH:17][c:18]([CH3:21])[cH:19][cH:20]2)[cH:14]1
ParticipantsSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 8028TetrahydrofuranHCID 16028TetrabutylammoniumHCID 28179Fluoride IonHCID 674598794-(4-Methylphenyl)-1-(4-methylphenyl)sulfonyl-3-phenylmethoxypyrazole

Product 1

HCID 178423892HCID 178423892, compound

Sources & evidence

ORD record
ord-d29ac80ae0d0485e9936114ee50a5644
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes