《Hydroxylation of benzene with hydrogen peroxide by the use of hydrophobic catechols and iron(3+) ion complexes as the catalyst》 was published in Chemistry Letters in 1981. These research results belong to Hotta, Kazuhiko; Tamagaki, Seizo; Suzuki, Yusuke; Tagaki, Waichiro. Synthetic Route of C10H14O2 The article mentions the following:
Hydroxylation of C6H6 with H2O2 was carried out in the presence of 3,4-( HO)2C6H3R (I; R = e.g., Me, Et, H, Bu, hexyl) and Fe3+ in a C6H6-H2O biphase system. The hydrophobic catechols I (R = Bu, hexyl, benzyl, PhCH2CH2) were far more effective as the catalyst than the hydrophilic ones.4-Butylbenzene-1,2-diol(cas: 2525-05-5Synthetic Route of C10H14O2) was used in this study.
4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry.Synthetic Route of C10H14O2 Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts