반응 #684168

ord-98bddf9858534e1c8000b0cc54589da6

반응 방정식

Cc1ccc(O)c(O)c1
1,2-dihydroxy-5-methylbenzene
OCC=Cc1ccccc1
cinnamyl alcohol
O=C1O[C@H]([C@@H](O)CO)C(O)=C1O
ascorbic acid
Cc1cc(O)c(O)cc1CC=Cc1ccccc1
4-cinnamyl-5-methyl-1,2-dihydroxybenzene
수율 49.6%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도at reflux for 20 hours
  2. 2
    온도After cooling
  3. 3
    기타an oily layer separated
  4. 4
    기타was collected
  5. 5
    workup.DISTILLATIONdistilled

실험 절차

A mixture of 1,2-dihydroxy-5-methylbenzene (124 g.) and cinnamyl alcohol (134 g.) in 2% aqueous citric acid (1.5 l.) containing ascorbic acid (10.0 g.) was boiled at reflux for 20 hours. After cooling, an oily layer separated and was collected and distilled to give 4-cinnamyl-5-methyl-1,2-dihydroxybenzene (119 g.) as a colorless oil, b.p. 205°-230° at 1.0 mm Hg. The oil was crystallized from a benzene/low-boiling petroleum ether (1/1) mixture to give colorless needles, m.p. 85°. Found: C, 79.9; H, 6.68. Calculated for C16H16O2 : C, 80.0; H, 6.71. The 100 MHz nuclear magnetic resonance (nmr) spectrum of this compound in deuterated chloroform exhibited a singlet (3 protons) at δ 2.07, a doublet (2 protons) at δ 3.37 (J = coupling constant = 5.0 Hz), a singlet (2 protons) at δ 5.02, a multiplet (2 protons) at δ 6.23-6.31, a singlet (1 proton) at δ 6.65, a singlet (1 proton) at δ 6.68, and a multiplet (5 protons) at δ 7.10-7.38.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04012529uspto-grants-1977_03