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Chloride → HCID 178501797, compound

HRID 140639
Notes
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Reaction equation

HRID 140639 reaction equation
[CH3:31][OH:32].[Cl-:39].[Cl:1][CH2:2][CH2:3][CH2:4][S:5](=[O:6])(=[O:7])[O:8][CH2:9][C:10]([CH:11]([C:12](=[O:13])[OH:14])[O:15][CH2:16][c:17]1[cH:18][cH:19][cH:20][cH:21][cH:22]1)([CH3:23])[CH3:24].[Cl:25][C:26]([C:27]([Cl:28])=[O:29])=[O:30].[Cl:40][CH2:41][Cl:42].[cH:33]1[cH:34][cH:35][n:36][cH:37][cH:38]1>>[Cl:1][CH2:2][CH2:3][CH2:4][S:5](=[O:6])(=[O:7])[O:8][CH2:9][C:10]([CH:11]([C:12](=[O:13])[O:14][CH3:26])[O:15][CH2:16][c:17]1[cH:18][cH:19][cH:20][cH:21][cH:22]1)([CH3:23])[CH3:24]
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 312ChlorideHCID 887MethanolHCID 1049PyridineHCID 6344DichloromethaneHCID 65578Oxalyl chlorideHCID 87453922(2R/S)-4-[(3-Chloropropyl)sulfonyloxy]-3,3-dimethyl-2-(phenylmethoxy)butanoic acid

Product 1

Sources & evidence

ORD record
ord-c4b6bbb742e54378a40506492be4ef73
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
HCID 178501797
HCID 178501797, compound