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Hydrochloric Acid → 5-(Cyclopent-1-enyl)-2-methylpentan-2-ol

HRID 2185164
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HRID 2185164 반응식
[C:1]1([CH2:6][CH2:7][CH2:8][C:9](=[O:11])[CH3:10])[CH2:5][CH2:4][CH2:3][CH:2]=1.[CH3:12][Mg]Br.Cl>C(OCC)C>[C:1]1([CH2:6][CH2:7][CH2:8][C:9]([CH3:12])([OH:11])[CH3:10])[CH2:5][CH2:4][CH2:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 135280095-(1-Cyclopentenyl)pentan-2-oneHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 184338735-(Cyclopent-1-enyl)-2-methylpentan-2-ol수율 11%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

5-(Cyclopent-1-enyl)-2-pentanone (5.95 g; 39 mmol) in ethyl ether (6 ml) was added dropwise to a 3M solution of methylmagnesium bromide in the same solvent (17 ml; 51 mmol) during 15 minutes. After 2 hours at reflux, the mixture was cooled down to room temperature, poured into ice (20 g), acidified with 5N HCl (20 ml) and extracted with MTBE (60 ml). The aqueous phase was separated and extracted again with MTBE (2×100 ml). The combined organic phases were washed with saturated NaHCO3 (80 ml), H2O (80 ml), brine (80 ml), dried over MgSO4 and concentrated in vacuo. Bulb-to-bulb distillation (80° C./0.06 torr) yielded quantitatively 5.84 g of 5-(cyclopent-1-enyl)-2-methylpentan-2-ol containing 11% of 5-cyclopentylidene-2-methylpentan-2-ol.

후처리

  1. temperatureAfter 2 hours at reflux
  2. extractionextracted with MTBE (60 ml)
  3. customThe aqueous phase was separated
  4. extractionextracted again with MTBE (2×100 ml)
  5. washThe combined organic phases were washed with saturated NaHCO3 (80 ml), H2O (80 ml), brine (80 ml)
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated in vacuo
  8. distillationdistillation (80° C./0.06 torr)

출처 및 근거

ORD 기록
ord-9586f4572e71411488278bbf89310e7c
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06399811B1

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