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Heptylundecanol → HCID 21225085, compound

HRID 358313
Notes
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Reaction equation

HRID 358313 reaction equation
CC(CC(C)(C)C)C[CH2:4][CH:5](C(C)CC(C)(C)C)[CH2:6][OH:7].[CH2:20]([CH:27]([CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38])[CH2:28][OH:29])[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]>>[CH2:4]([O:29][CH2:28][CH:27]([CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38])[CH:5]1[O:7][CH2:6]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 95338HeptylundecanolHCID 2563715,7,7-Trimethyl-2-(1,3,3-trimethylbutyl)-1-octanol

Product 1

HCID 21225085HCID 21225085, compoundYield 80%

Procedure

The same reaction as in Reference Example 1 was carried out under the same conditions except that the 5,7,7-trimethyl-2-(1,3,3-trimethylbutyl) octanol in Reference Example 1 was replaced by 2-heptylundecanol, whereupon 65 g (yield: 80%) of 2-heptylundecyl glycidyl ether was obtained.

Workup

  1. customThe same reaction as in Reference Example 1

Sources & evidence

ORD record
ord-1552ff0de7734ead9de78bfdf1ceacd0
Source dataset
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04465869

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes