HCID 75995668, compound → HCID 131731337, compound

HRID 2369271Notes

Reaction equation

HRID 2369271 reaction equation
[CH3:1][C:2]([CH2:17][CH2:18][CH2:19][CH:20]([CH3:32])[CH2:21][CH2:22][CH2:23][CH:24]([CH3:31])[CH2:25][CH2:26][CH2:27][CH:28]([CH3:30])[CH3:29])=[CH:3][CH2:4][CH2:5][C:6]([O:8][CH2:9][C:10]([CH2:15][OH:16])([CH2:13][OH:14])[CH2:11][OH:12])=[O:7]>O>[CH3:1][C:2]([CH2:17][CH2:18][CH2:19][CH:20]([CH3:32])[CH2:21][CH2:22][CH2:23][CH:24]([CH3:31])[CH2:25][CH2:26][CH2:27][CH:28]([CH3:30])[CH3:29])=[CH:3][CH2:4][CH2:5][C:6]([O:8][CH2:9][C:10]([CH2:13][OH:14])([CH2:11][OH:12])[CH2:15][OH:16])=[O:7].[OH2:7]

Participants

3

Reactant 1

HCID 75995668HCID 75995668, compound2×

Product 1

HCID 131731337HCID 131731337, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol and pure water were introduced into a mixing device at the concentration of 50 wt % Mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol (water-excess condition), and incubation thereof was carried out while performing 100 or more times of mixing operations at room temperature (25° C.) over the period of 24 hours. Thus, a homogeneously mixed sample of mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol/water system was obtained. This sample of mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol/water system appeared to be a white turbid gel composition.

Workup

  1. customat room temperature
  2. custom(25° C.)
  3. customover the period of 24 hours

Sources & evidence

ORD record
ord-97081104f00448959891df9d17f521e9
Source dataset
uspto-grants-2014_04
Patent number
US08703922B2

Reaction notes

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