Dimethyl Sulfoxide → HCID 21059936, compound

HRID 106089Notes

Reaction equation

HRID 106089 reaction equation
[CH3:1][S:2](=[O:3])[CH3:4].[CH3:38][CH2:39][N:40]([CH2:41][CH3:42])[CH2:43][CH3:44].[CH3:48][CH2:49][O:50][C:51](=[O:52])[CH3:53].[Cl:45][CH2:46][Cl:47].[Cl:5][C:6]([C:7]([Cl:8])=[O:9])=[O:10].[O:11]1[CH2:12][O:13][c:14]2[c:15]1[cH:16][cH:17][c:18]([CH:20]([CH2:21][C:22](=[O:23])[O:24][CH2:25][CH3:26])[CH2:27][c:28]1[n:29][c:30]([CH2:33][CH2:34][CH2:35][CH2:36][OH:37])[s:31][cH:32]1)[cH:19]2>>[O:11]1[CH2:12][O:13][c:14]2[c:15]1[cH:16][cH:17][c:18]([CH:20]([CH2:21][C:22](=[O:23])[O:24][CH2:25][CH3:26])[CH2:27][c:28]1[n:29][c:30]([CH2:33][CH2:34][CH2:35][CH:36]=[O:37])[s:31][cH:32]1)[cH:19]2

Participants

7

Reactant 6

HCID 679Dimethyl SulfoxideHCID 6344DichloromethaneHCID 8471TriethylamineHCID 8857Ethyl AcetateHCID 65578Oxalyl chlorideHCID 21059937HCID 21059937, compound

Product 1

HCID 21059936HCID 21059936, compound

Sources & evidence

ORD record
ord-57dac62d302a45edb8bb8c80afd1a769
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction notes

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