تفاعل #55054

ord-3ebd2558f3104815a5ab360475dfe70b

معادلة التفاعل

CC(C)CCC[C@@H](C)CC(=O)C[C@@H](C)CO
(2R,6R)-1-hydroxy-2,6,10-trimethylundecan-4-one
[K+].[OH-]
KOH
NN.O
hydrazine hydrate
CC(C)CCC[C@@H](C)CCC[C@@H](C)CO
(2R,6R)-(+)-2,6,10-trimethylundecan-1-ol

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONA mixture of 3.98 g
  2. 2
    درجة الحرارةheated until distillation
  3. 3
    workup.DISTILLATIONDistillation
  4. 4
    أخرىreached 195° C.
  5. 5
    درجة الحرارةat reflux for 4 hours
  6. 6
    درجة الحرارةAfter cooling
  7. 7
    workup.ADDITIONthe resulting mixture was treated with ice and 3 N aqueous HCl
  8. 8
    استخلاصworked-up by ether extraction in the manner of Example 1 giving 2.9 g
  9. 9
    أخرىThis material was chromatographed on 180 g
  10. 10
    غسيلElution with 4:1 parts by volume hexane-ether

الإجراء التجريبي

A mixture of 3.98 g. (0.0174 mole) of (2R,6R)-1-hydroxy-2,6,10-trimethylundecan-4-one, 108 ml. of diethylene glycol, 25 g. of KOH and 43.5 ml. of hydrazine hydrate was stirred and heated until distillation began. Distillation was then continued until the internal temperature of the reaction mixture reached 195° C. then the mixture was mintained at reflux for 4 hours. After cooling, the resulting mixture was treated with ice and 3 N aqueous HCl and worked-up by ether extraction in the manner of Example 1 giving 2.9 g. of a pale yellow oil. This material was chromatographed on 180 g. of silica gel. Elution with 4:1 parts by volume hexane-ether yielded (2R,6R)-(+)-2,6,10-trimethylundecan-1-ol which was evaporatively distilled affording 2.22 g. of a colorless oil, b.p. 90°-105° C. (bath temperature) (0.2 mm Hg.); [α]25D+ 9.44° (c 2.04, hexane).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04151205uspto-grants-1979_04