Acetonitrile → HCID 22989453, compound

HRID 2131309Notes

Reaction equation

HRID 2131309 reaction equation
[C:31](#[N:32])[CH3:33].[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][C:9](=[O:10])[N:11]1[CH2:12][CH2:13][C:14]([CH2:17][CH2:18][OH:19])([CH2:20][CH2:21][OH:22])[CH2:15][CH2:16]1.[CH2:34]([Cl:35])[Cl:36].[CH3:23][N+:24]1([O-:25])[CH2:26][CH2:27][O:28][CH2:29][CH2:30]1.[CH3:42][CH2:43][CH2:44][N+:45]([CH2:46][CH2:47][CH3:48])([CH2:49][CH2:50][CH3:51])[CH2:52][CH2:53][CH3:54].[O-:37][Ru:38](=[O:39])(=[O:40])=[O:41]>>[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][C:9](=[O:10])[N:11]1[CH2:12][CH2:13][C:14]2([CH2:15][CH2:16]1)[CH2:17][C:18](=[O:19])[O:22][CH2:21][CH2:20]2

Participants

7

Reactant 6

HCID 6342AcetonitrileHCID 6344DichloromethaneHCID 9559TetrapropylammoniumHCID 82029Methyl morpholine oxideHCID 22989502Phenylmethyl 4,4-bis(2-hydroxyethyl)-1-piperidinecarboxylateHCID 178527104HCID 178527104, compound

Product 1

HCID 22989453HCID 22989453, compound

Sources & evidence

ORD record
ord-d80eadd3144a48069bace49792dbc149
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

Loading…