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Hydroxide → 2-Trifluoromethylsulfonyloxy-4-pyridinyl 4,4,4-trifluoro-1-butanesulfonate

HRID 2350238
Notes
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Reaction equation

HRID 2350238 reaction equation
[CH2:17]([N+:18]([CH2:19][CH2:20][CH2:21][CH3:22])([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:27][CH2:28][CH2:29][CH3:30])[CH2:31][CH2:32][CH3:33].[Cl:45][CH2:46][Cl:47].[F:1][C:2]([S:3](=[O:4])(=[O:5])[O:6][c:7]1[n:8][cH:9][cH:10][c:11]([OH:13])[cH:12]1)([F:14])[F:15].[F:34][C:35]([CH2:36][CH2:37][CH2:38][S:39](=[O:40])(=[O:41])[Cl:42])([F:43])[F:44].[OH-:16].[OH2:48]>>[F:1][C:2]([S:3](=[O:4])(=[O:5])[O:6][c:7]1[n:8][cH:9][cH:10][c:11]([O:13][S:39]([CH2:38][CH2:37][CH2:36][C:35]([F:34])([F:43])[F:44])(=[O:40])=[O:41])[cH:12]1)([F:14])[F:15]
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 961HydroxideHCID 962WaterHCID 6344DichloromethaneHCID 16028TetrabutylammoniumHCID 27611764,4,4-trifluorobutane-1-sulfonyl ChlorideHCID 178527628HCID 178527628, compound

Product 1

HCID 20816522
2-Trifluoromethylsulfonyloxy-4-pyridinyl 4,4,4-trifluoro-1-butanesulfonate

Sources & evidence

ORD record
ord-e443242124464be78dc724b451ef815c
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