Diisopropylamine → HCID 86743623, compound

HRID 477642Notes

Reaction equation

[CH2:1]([O:3][C:4]([CH:6]=[C:7]([CH3:31])[CH2:8][CH2:9][CH:10]=[C:11]([CH3:30])[CH2:12][CH2:13][CH:14]=[C:15]([CH3:29])[CH2:16][CH2:17][CH:18]=[C:19]([CH3:28])[CH2:20][CH2:21][CH:22]=[C:23]([CH3:27])[C:24]([OH:26])=O)=[O:5])[CH3:2].[CH:32]([NH:35][CH:36]([CH3:38])[CH3:37])([CH3:34])[CH3:33]>>[CH2:1]([O:3][C:4]([CH:6]=[C:7]([CH3:31])[CH2:8][CH2:9][CH:10]=[C:11]([CH3:30])[CH2:12][CH2:13][CH:14]=[C:15]([CH3:29])[CH2:16][CH2:17][CH:18]=[C:19]([CH3:28])[CH2:20][CH2:21][CH:22]=[C:23]([CH3:27])[C:24]([N:35]([CH:36]([CH3:38])[CH3:37])[CH:32]([CH3:34])[CH3:33])=[O:26])=[O:5])[CH3:2]

Participants

Reactant 2

HCID 7912Diisopropylamine

HCID 53741409HCID 53741409, compound

Product 1

HCID 86743623HCID 86743623, compound

Procedure

Starting materials: 19-ethoxycarbonyl-2,6,10,14,18-pentamethyl-2,6,10,14,18-nonadecapentaenoic acid and diisopropylamine.

Sources & evidence

ORD record: ord-87d96265ece84ba79af82641858b2341
Source dataset: uspto-grants-1989_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04888439

Reaction notes

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