تفاعل #55734

ord-c9d0b6db7a5e4cd096ceeaf647c74a38

معادلة التفاعل

CCCCCC.c1ccccc1
benzene hexane
C/C(=C\CO)CCC[C@H](C)CCC[C@H](C)CCCC(C)C
Phytol
[H][H]
hydrogen
→
CC(C)CCCC(C)CCCC(C)CCCC(C)CCO
title compound
المردود 82.3%
CC(C)CCCC(C)CCCC(C)CCCC(C)CCO
dihydrophytol
المردود 82.3%

المتفاعلات

CCCCCC.c1ccccc1
benzene hexane
C/C(=C\CO)CCC[C@H](C)CCC[C@H](C)CCCC(C)C
Phytol
[H][H]
hydrogen

الكواشف

[Ni]
Ni

المذيبات

CCO
ethanol
CCO
ethanol

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    أخرىwas absorbed
  3. 3
    ترشيحAfter filtering off the catalyst through a filter paper
  4. 4
    أخرىthe ethanol was evaporated

الإجراء التجريبي

Phytol (30.0 g, 0.101 mol) was dissolved in 200 ml of ethanol. A suspension of 1.8 g of Raney-Ni (W-1) in 5 ml of ethanol was added thereto, and hydrogenation was carried out under hydrogen for about 5 hours so that 2405 ml of hydrogen (theoretical volume at 24° C.; 2465 ml) was absorbed. After filtering off the catalyst through a filter paper, the ethanol was evaporated. Yield 29.9 g. Silica gel column chromatography with benzene-hexane (1:1) gave 24.7 g of the title compound (yield 82.3%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04221810uspto-grants-1980_09