Potassium Hydroxide → (2R,6R)-(+)-2,6,10-trimethylundecan-1-ol

HRID 1701238Notes

Reaction equation

HRID 1701238 reaction equation
[OH:1][CH2:2][C@H:3]([CH3:16])[CH2:4][C:5](=O)[CH2:6][C@H:7]([CH3:14])[CH2:8][CH2:9][CH2:10][CH:11]([CH3:13])[CH3:12].[OH-].[K+].O.NN>C(O)COCCO>[CH3:16][C@H:3]([CH2:4][CH2:5][CH2:6][C@H:7]([CH3:14])[CH2:8][CH2:9][CH2:10][CH:11]([CH3:13])[CH3:12])[CH2:2][OH:1]

Participants

5

Procedure

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 maintained 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).

Workup

  1. additionA mixture of 3.98 g
  2. temperatureheated until distillation
  3. distillationDistillation
  4. customreached 195° C.
  5. temperaturethe mixture was maintained
  6. temperatureat reflux for 4 hours
  7. temperatureAfter cooling
  8. additionthe resulting mixture was treated with ice and 3 N aqueous HCl
  9. extractionworked-up by ether extraction in the manner of Example 1 giving 2.9 g
  10. customThis material was chromatographed on 180 g
  11. washElution with 4:1 parts by volume hexane-ether

Sources & evidence

ORD record
ord-f8c090d68050442798eac25931cd5971
Source dataset
uspto-grants-1980_03
Patent number
US04191842

Reaction notes

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