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Diethylene Glycol Monoethyl Ether → Ethylene brassylate

HRID 1074631
Notes
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Reaction equation

HRID 1074631 reaction equation
[C:1]([O-:20])(=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]CCCCC.[Na+].[C:22]([O-])(=[O:40])[CH2:23]CCCCCCCCCCCCCCCC.[K+].C([O:45]CCOCCO)C>>[C:13]1(=[O:45])[O:40][CH2:22][CH2:23][O:20][C:1](=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 8146Diethylene Glycol Monoethyl EtherHCID 2724691Sodium StearateHCID 23673840Potassium Stearate

Product 1

HCID 61014Ethylene brassylateYield 73.2%

Procedure

A mixed metal catalyst prepared similarly to that of Example X, except that sodium stearate was substituted for the potassium stearate and ethyl cellusolve replaced with diethylene glycol monoethyl ether, was employed for the continuous depolymerization of poly(ethylene brassylate) in accordance with the procedure and conditions of Example I. Ethylene brassylate was continuously produced and distilled from the reactor at a rapid rate and the overall yield was 73.2%. Comparable results are obtained with a catalyst comprised of sodium benzoate and aluminum tricellusolve (Al(OCH2CH2OC2H5)3).

Workup

  1. customA mixed metal catalyst prepared similarly to that of Example X

Sources & evidence

ORD record
ord-4a23ea2bd1114aa0b97a9174535b9e69
Source dataset
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04393223

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes