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Cyclopentylidenecyclopentan-2-one → Cyclopentanol, 2-cyclopentylidene-

HRID 1955571
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HRID 1955571 반응식
[C:1]1(=[C:6]2[CH2:10][CH2:9][CH2:8][C:7]2=[O:11])[CH2:5][CH2:4][CH2:3][CH2:2]1.[BH4-].[Na+]>CO>[C:1]1(=[C:6]2[CH2:10][CH2:9][CH2:8][CH:7]2[OH:11])[CH2:2][CH2:3][CH2:4][CH2:5]1
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참가 물질

4

반응물 2

HCID 69995Cyclopentylidenecyclopentan-2-oneHCID 4311764Sodium borohydride

생성물 1

HCID 579236Cyclopentanol, 2-cyclopentylidene-수율 106.1%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A 2 liter round bottom flask, fitted with a mechanical stirrer, a reflux condenser and a thermometer, was charged with 412.4 g (2.75 mol) of 2-Cyclopentylidene-cyclopentanone and 500 ml methanol. The mixture was stirred until homogeneous at room temperature and then 40 g of sodium borohydride was added in small portions over a period of 1.5 hour. The reaction mixture was thereafter stirred for another 4 hours. During addition as well as thereafter the temperature was kept below 40° C. by cooling with a cold water bath if necessary. The reaction mixture was further stirred overnight. Thereafter it was quenched by dropwise addition, with stirring, of 250 ml of water. The aqueous and organic layers were separated and the aqueous layer extracted twice with 200 ml diethyl ether. The combined organic layers were washed with 200 ml water and dried over magnesium sulphate. After filtration the solvent was removed using a rotary evaporator and 444 g of crude product were obtained. This was fractioned under reduced pressure (0.4 kPa) through a 0.5 meter Sulzer-packed column. Fractions were collected at 90°-100° C. and odour assessed. The total of fractions with an acceptable odour was 182.9 g. The product could be further purified by recristallization from methanol.

후처리

  1. customA 2 liter round bottom flask, fitted with a mechanical stirrer, a reflux condenser
  2. stirringThe reaction mixture was thereafter stirred for another 4 hours
  3. additionDuring addition as well as thereafter the temperature
  4. customwas kept below 40° C.
  5. temperatureby cooling with a cold water bath if necessary
  6. customThereafter it was quenched by dropwise addition
  7. stirringwith stirring, of 250 ml of water
  8. customThe aqueous and organic layers were separated
  9. extractionthe aqueous layer extracted twice with 200 ml diethyl ether
  10. washThe combined organic layers were washed with 200 ml water
  11. dry with materialdried over magnesium sulphate
  12. filtrationAfter filtration the solvent
  13. customwas removed
  14. customa rotary evaporator

출처 및 근거

ORD 기록
ord-f643ddeb6f344446bf859a3bf05f19d9
출처 데이터셋
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05776884

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