Disobutylphenol Synthesis-Structure-Properties-Derivatives

Niederl, Joseph B.

doi:10.1021/ie50347a014

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Solutions and Reagents1

■ Introduction1

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1942

2016

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Cited by 16 publications

(2 citation statements)

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“…2 -Hydroxy' -5 -(1,1,3,3 -tetramethylbutyll-cri.cP-xylenediol. Prepared from p-( 1,1,3,3-tetramethylbutyl)-phenol and formaldehyde (14). Recrystallized three times from petroleum ether; melting point 71°.…”

Section: Solutions and Reagentsmentioning

confidence: 99%

Bromination of Phenols and Phenol Alcohols

Ruderman¹

1946

Ind. Eng. Chem. Anal. Ed.

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Section: Solutions and Reagentsmentioning

confidence: 99%

Bromination of Phenols and Phenol Alcohols

Ruderman¹

1946

Ind. Eng. Chem. Anal. Ed.

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“…In 1938, the technology of 4-TOPhs synthesis was developed in the USA. 1 The process is represented by phenol alkylation with diisobutylene (DIB) at 288−308 K in the presence of H 2 SO 4 (7% mass.). A ratio of DIB to H 2 SO 4 (7% mass) was 1:1.…”

Section: ■ Introductionmentioning

confidence: 99%

Theory and Practice of Alkyl Phenol Synthesis. tert-Octylphenols

Krymkin

Shakun

Nesterova

et al. 2016

Ind. Eng. Chem. Res.

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Liquid-phase alkylation of phenol with diisobutylenes was studied in the presence of ion-exchange resin Amberlyst 36 Dry. Thermodynamic characteristics were calculated for the reactions that occur in a reaction system. Kinetics of the alkylation process was studied. The conditions of selective synthesis were recommended for 4-tert-octylphenol. Recommendations on the use of obtained data were given.

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Studien auf dem Gebiete der Phenol‐Formaldehyd‐Harze, IX. Mitteil.: Zur Bildung von Aldehydgruppen beim Aushärten einiger Phenoldialkohole

Hultzsch¹,

Schiemann²

1942

Ber. dtsch. Chem. Ges. A/B

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Disobutylphenol Synthesis-Structure-Properties-Derivatives

Cited by 16 publications

References 22 publications

Bromination of Phenols and Phenol Alcohols

Bromination of Phenols and Phenol Alcohols

Theory and Practice of Alkyl Phenol Synthesis. tert-Octylphenols

Studien auf dem Gebiete der Phenol‐Formaldehyd‐Harze, IX. Mitteil.: Zur Bildung von Aldehydgruppen beim Aushärten einiger Phenoldialkohole

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