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Water → 5-Methylene-2-(4-trifluoromethoxy-phenyl)-hexahydro-cyclopenta[c]pyrrol-1-one

HRID 1887496
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HRID 1887496 반응식
O[CH:2]1[N:6]([C:7]2[CH:12]=[CH:11][C:10]([O:13][C:14]([F:17])([F:16])[F:15])=[CH:9][CH:8]=2)[C:5](=[O:18])[CH:4]2[CH2:19][C:20](=[CH2:22])[CH2:21][CH:3]12.[BH3-]C#N.[Na+].O>FC(F)(F)C(O)=O>[CH2:22]=[C:20]1[CH2:19][CH:4]2[C:5](=[O:18])[N:6]([C:7]3[CH:8]=[CH:9][C:10]([O:13][C:14]([F:16])([F:15])[F:17])=[CH:11][CH:12]=3)[CH2:2][CH:3]2[CH2:21]1
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참가 물질

5

반응물 3

HCID 962WaterHCID 5003444Sodium cyanoborohydrideHCID 866739173-Hydroxy-5-methylene-2-(4-trifluoromethoxy-phenyl)-hexahydro-cyclopenta[c]pyrrol-1-one

생성물 1

HCID 866739185-Methylene-2-(4-trifluoromethoxy-phenyl)-hexahydro-cyclopenta[c]pyrrol-1-one수율 42%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

To a solution of 3-Hydroxy-5-methylene-2-(4-trifluoromethoxy-phenyl)-hexahydro-cyclopenta[c]pyrrol-1-one (0.1 g, 0.32 mmol) in trifluoroacetic acid (20 mL) was added NaCNBH3 (0.04 g, 0.64 mmol) at −20° C., and the mixture was stirred for 1 h. Water (30 mL) was added. The mixture was extracted with dichloromethane (3×20 mL), washed with brine (50 mL), and dried over anhydrous Na2SO4. The solvent was removed by reduced pressure. The residue was purified by column chromatography on silica gel with petroleum ether/ethyl acetate (10:1 to 5:1) to yield the title compound (40 mg, 40%). 1H NMR (300 MHz, CDCl3): δ 7.69-7.64 (m, 2H), 7.25-7.19 (m, 2H), 4.91 (s, 2H), 4.07-4.01 (m, 1H), 3.54-3.49 (m, 1H), 3.19-3.12 (m, 1H), 2.96-2.71 (m, 4H), 2.25-2.18 (m, 1H); LC-MS: [M+1]+ 298.1.

후처리

  1. extractionThe mixture was extracted with dichloromethane (3×20 mL)
  2. washwashed with brine (50 mL)
  3. dry with materialdried over anhydrous Na2SO4
  4. customThe solvent was removed by reduced pressure
  5. customThe residue was purified by column chromatography on silica gel with petroleum ether/ethyl acetate (10:1 to 5:1)

출처 및 근거

ORD 기록
ord-394849c6648e4970b4d9061722407a28
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501768B2

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