Hexane → 2,2-Ethylenedioxy-6-formyl-10-methyl-5,9-undecadiene

HRID 1439455노트

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HRID 1439455 반응식
[Br-].[CH2:2]1[CH2:29][O:28][C:4]([CH3:27])([CH2:5][CH2:6][CH2:7][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[O:3]1.C([Li])CCC.CCCCCC.C([O:43][CH:44](OCC)[C:45](=O)[CH2:46][CH2:47][CH:48]=[C:49]([CH3:51])[CH3:50])C.CCCCCC>O1CCCC1.C(O)(=O)C>[CH2:29]1[CH2:2][O:3][C:4]([CH2:5][CH2:6][CH:7]=[C:45]([CH:44]=[O:43])[CH2:46][CH2:47][CH:48]=[C:49]([CH3:51])[CH3:50])([CH3:27])[O:28]1

참가 물질

7

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온도
-60 °C

실험 절차

In 160 ml of anhydrous tetrahydrofuran was suspended 38.5 g of 4,4-ethylenedioxypentan-1-yltriphenylphosphonium bromide, and to this was added the equimolar amount of a n-butyl-lithium-hexane solution at -20° C in a stream of nitrogen. The reaction mixture was stirred for 1 hour and cooled to -60° C. To this was added 14.5 g of 1,1-diethoxy-6-methyl-5-hepten-2-one, and the resulting mixture was stirred at room temperature for 3 hours. The reaction mixture was, after addition of ice-water, extracted with n-hexane and from the extract was obtained an oil. The oil was suspended in 250 ml of 50 % acetic acid and stirred at room temperature for one hour. 2,2-Ethylenedioxy-6-formyl-10-methyl-5,9-undecadiene obtained by the n-hexane extraction, not purified, was reduced in 100 ml of ethanol by using 500 mg of sodium borohydride. The product thus obtained was chromatographed on the silica gel (100 g) column to yield 7.3 g of 2,2-ethylenedioxy-6-hydroxymethyl-10-methyl-5,9-undecadien.

후처리

  1. stirringthe resulting mixture was stirred at room temperature for 3 hours
  2. extractionextracted with n-hexane and from the extract
  3. customwas obtained an oil
  4. stirringstirred at room temperature for one hour

출처 및 근거

ORD 기록
ord-b474e673e60a4d21b8e512ef566150b4
출처 데이터셋
uspto-grants-1977_11
특허 번호
US04059641

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