Water → HCID 21474587, 화합물

HRID 1756421노트

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HRID 1756421 반응식
[CH3:1][C:2]1([CH3:19])[CH2:11][CH2:10][C:9]([CH3:13])([CH3:12])[C:8]2[CH:7]=[C:6]([C:14](=[O:18])[C:15]([OH:17])=[O:16])[CH:5]=[CH:4][C:3]1=2.[CH2:20]1COCC1.C([Mg]I)C.O>C(OCC)C>[OH:18][C:14]([C:6]1[CH:5]=[CH:4][C:3]2[C:2]([CH3:19])([CH3:1])[CH2:11][CH2:10][C:9]([CH3:12])([CH3:13])[C:8]=2[CH:7]=1)([CH3:20])[C:15]([OH:17])=[O:16]

참가 물질

6

반응물 4

HCID 962WaterHCID 8028TetrahydrofuranHCID 12051800HCID 12051800, 화합물HCID 178461634HCID 178461634, 화합물

생성물 1

HCID 21474587HCID 21474587, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

3.1 g (12 mmol) of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthylglyoxylic acid and 50 ml of THF are introduced into a three-necked flask. At 0° C. and under a stream of nitrogen, 16 ml (48 retool) of a solution of ethylmagnesium iodide in ethyl ether (3M) are added dropwise and the mixture is stirred at room temperature for four hours. The reaction medium is poured into water, the mixture is extracted with ethyl ether and the organic phase is separated after settling has taken place, then dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a silica column and eluted with a mixture of dichloromethane and ethyl ether (20:80). After evaporation of the solvents, 2.6 g (79%) of the expected product, melting point 168°-169° C., are collected.

후처리

  1. extractionthe mixture is extracted with ethyl ether
  2. customthe organic phase is separated after settling
  3. dry with materialdried over magnesium sulphate
  4. customevaporated
  5. customThe residue obtained
  6. customis purified by chromatography on a silica column
  7. washeluted with a mixture of dichloromethane and ethyl ether (20:80)
  8. customAfter evaporation of the solvents, 2.6 g (79%) of the expected product, melting point 168°-169° C.
  9. customare collected

출처 및 근거

ORD 기록
ord-65ff4a7df1f542cdae2ecd90533a09db
출처 데이터셋
uspto-grants-1995_08
특허 번호
US05439925

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