Water → HCID 178455744, 화합물

HRID 1982116노트

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HRID 1982116 반응식
Br[C:2](Br)=[CH:3][C@H:4]1[CH2:9][CH2:8][C@H:7]([CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH2:6][CH2:5]1.C([Li])CCC.O>O1CCCC1.CCCCCC>[C:3]([C@H:4]1[CH2:9][CH2:8][C@H:7]([CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH2:6][CH2:5]1)#[CH:2]

참가 물질

6

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온도
-70 °C

실험 절차

A solution of 35.9 g of trans-1-(2,2-dibromovinyl)-4-pentylcyclohexane in 300 ml of absolute tetrahydrofuran at -70° C. was placed under argon gasification and treated within 20 minutes with 222 ml of a 1.2M solution of butyl lithium in hexane. The mixture was subsequently stirred at -70° C. for a further 2 hours, then poured into 1.2 l of water and extracted three times with 400 ml of hexane each time. The organic phases were washed twice with 400 ml of water each time, dried over magnesium sulphate and concentrated. Crystallization of the residue (19.4 g) from 250 ml of methanol at -78° C. gave 10.0 g of trans-1-ethynyl-4-pentylcyclohexane which was a colourless liquid at room temperature. Crystallization of the mother liquor, concentrated to about 100 ml, at -78° C. gave a further 3.9 g of trans-1-ethynyl-4-pentylcyclohexane. The combined batches of product were crystallized again from 300 ml of methanol at -78° C. and subsequently distilled (110° C./0.3 Torr), there being obtained 10.43 g (55%) of trans-1-ethynyl-4-pentylcyclohexane (purity 99.4%) as a colourless liquid; Rf-value (hexane) 0.41.

후처리

  1. customat -70° C.
  2. extractionextracted three times with 400 ml of hexane each time
  3. washThe organic phases were washed twice with 400 ml of water each time
  4. dry with materialdried over magnesium sulphate
  5. concentrationconcentrated
  6. customCrystallization of the residue (19.4 g) from 250 ml of methanol at -78° C.

출처 및 근거

ORD 기록
ord-575348bfd5ec46fcbed5f023fe4c18d7
출처 데이터셋
uspto-grants-1986_06
특허 번호
US04595521

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