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Cyclohexanecarbonyl chloride → 4-[1-(Cyclohexanoyloxy)tridecyl]-2-trimethylsilylfuran

HRID 1109871
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HRID 1109871 반응식
C([Li])(C)(C)C.[OH:6][CH:7]([C:20]1[CH:21]=[C:22]([Si:25]([CH3:28])([CH3:27])[CH3:26])[O:23][CH:24]=1)[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19].[CH:29]1([C:35](Cl)=[O:36])[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1>CCCCC.O1CCCC1>[CH:29]1([C:35]([O:6][CH:7]([C:20]2[CH:21]=[C:22]([Si:25]([CH3:28])([CH3:27])[CH3:26])[O:23][CH:24]=2)[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])=[O:36])[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1
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참가 물질

6

반응물 3

HCID 75938Cyclohexanecarbonyl chlorideHCID 156632683-(1-Hydroxytridecyl)-5-trimethylsilylfuranHCID 178418306HCID 178418306, 화합물

생성물 1

HCID 150370664-[1-(Cyclohexanoyloxy)tridecyl]-2-trimethylsilylfuran

시약·촉매·용매 2

HCID 8003Pentane용매HCID 8028Tetrahydrofuran
용매

실험 절차

tert-Butyl lithium (a 1.7 M solution in pentane; 0.33 ml, 0.55 mmol) was added dropwise to a solution of 4-(1-hydroxytridecyl)-2-trimethylsilylfuran (170 mg, 0.50 mmol) in tetrahydrofuran (5 ml) at 0 degrees under argon. After 10 minutes, cyclohexanecarboxylic acid chloride (74 microliter, 0.55 mmol) was added. The mixture was stirred at room temperature for 15 hours and quenched with water. Extraction and evaporation of the dried (magnesium sulphate) extracts gave an oil, which was purified by preparative TLC (20×20 cm, 1000 u silica plate; developed with 5% ethyl ether/hexane). The title ester was obtained as a pale yellow oil.

후처리

  1. customquenched with water
  2. extractionExtraction and evaporation of the
  3. dry with materialdried (magnesium sulphate)
  4. customextracts gave an oil, which
  5. customwas purified by preparative TLC (20×20 cm, 1000 u silica plate; developed with 5% ethyl ether/hexane)

출처 및 근거

ORD 기록
ord-d7563b0c3014410291961d3a4bfbf636
출처 데이터셋
uspto-grants-1994_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05322953

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