6-tert-Butyl-4-[(dimethylamino)methyl]-2,3-dimethylphenol → HCID 20361470, compound

HRID 1679781Notes

Reaction equation

HRID 1679781 reaction equation
[CH2:1]([O:19][C:20](=[O:61])[CH:21]([CH2:43][C:44]1[CH:49]=[C:48]([C:50]([CH2:53]C(C)(C)C)([CH3:52])[CH3:51])[C:47](O)=[C:46]([CH3:59])[C:45]=1[CH3:60])[C:22]([O:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH3:42])=[O:23])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].C(C1C([OH:72])=C(C)C(C)=C(CN(C)C)C=1)(C)(C)C>>[CH2:1]([O:19][C:20](=[O:61])[CH:21]([CH:43]([OH:72])[C:44]1[CH:49]=[C:48]([C:50]([CH3:53])([CH3:52])[CH3:51])[CH:47]=[C:46]([CH3:59])[C:45]=1[CH3:60])[C:22]([O:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH3:42])=[O:23])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]

Participants

3

Reactant 2

HCID 221015906-tert-Butyl-4-[(dimethylamino)methyl]-2,3-dimethylphenolHCID 86735586HCID 86735586, compound

Product 1

HCID 20361470HCID 20361470, compound

Procedure

Di-n-octadecyl(5-tert.-octyl-2,3-dimethyl-4-hydroxybenzyl)malonate was made in a similar manner to that of Example 5 by substituting the intermediate of Example 2 for 6-tert.-butyl-2,3-dimethyl-4-(dimethylaminomethyl)phenol (Example 1).

Sources & evidence

ORD record
ord-41b9fa55d15845898472e9c16f791512
Source dataset
uspto-grants-1978_03
Patent number
US04081475

Reaction notes

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