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71623-60-4 → Lauric Acid

HRID 1466468
Notes
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Reaction equation

HRID 1466468 reaction equation
[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]([O:14][CH2:15][C@@H:16]([OH:25])[C@H:17]1[O:22][C:20](=[O:21])[C:19]([OH:23])=[C:18]1[OH:24])=[O:13]>C(#N)C>[CH2:15]([OH:14])[C@@H:16]([OH:25])[C@H:17]1[O:22][C:20](=[O:21])[C:19]([OH:23])=[C:18]1[OH:24].[C:12]([OH:14])(=[O:13])[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH3:1]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 10228286371623-60-4

Product 2

HCID 3893Lauric AcidYield 99%HCID 54675810Erythorbic AcidYield 99%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

Erythorbic acid (≧99.0%, Fluka, Sigma-Aldrich) and lauric acid (≧99.0%, Fluka, Sigma-Aldirch) were prepared as raw materials for the synthesis of erythorbyl laurate, and acetonitrile (J. T. Baker Co., Philips burg, NJ USA) was used.

Sources & evidence

ORD record
ord-7f43123b523343229ea5d7ca4bb03dab
Source dataset
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09000034B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes