tert-Butanol → HCID 21388034, compound

HRID 1119610Notes

Reaction equation

HRID 1119610 reaction equation
[C:28]([CH3:29])([CH3:30])([CH3:31])[N:32]1[CH:33]([c:39]2[cH:40][cH:41][cH:42][cH:43][cH:44]2)[O:34][CH:35]([CH2:37][OH:38])[CH2:36]1.[C:45]([OH:46])([CH3:47])([CH3:48])[CH3:49].[Cl:15][c:16]1[c:17]2[c:18]([cH:19][cH:20][c:21]([Cl:22])[cH:23]2)[cH:24][c:25]([CH3:26])[n:27]1.[Cl:2][c:3]1[n:4][cH:5][c:6]([CH3:14])[c:7]2[cH:8][cH:9][c:10]([Cl:13])[cH:11][c:12]12.[K:1]>>[c:3]1([O:38][CH2:37][CH:35]2[O:34][CH:33]([c:39]3[cH:40][cH:41][cH:42][cH:43][cH:44]3)[N:32]([C:28]([CH3:29])([CH3:30])[CH3:31])[CH2:36]2)[n:4][cH:5][c:6]([CH3:14])[c:7]2[cH:8][cH:9][c:10]([Cl:13])[cH:11][c:12]12

Participants

6

Reactant 5

HCID 6386tert-ButanolHCID 1088103-(1,1-Dimethylethyl)-2-phenyloxazolidine-5-methanolHCID 5462222PotassiumHCID 21388031HCID 21388031, compoundHCID 213880331,7-Dichloro-3-methylisoquinoline

Product 1

HCID 21388034HCID 21388034, compound

Sources & evidence

ORD record
ord-79fa26f644114cdcb69a00047912f87c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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