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Formaldehyde → HCID 11596500, 화합물

HRID 1360019
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HRID 1360019 반응식
[CH3:1][O:2][C:3](=[O:28])/[C:4](/[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[CH2:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([NH:22][CH2:23][CH:24]([CH3:26])[CH3:25])=[CH:18][C:17]=1[F:27])=[CH:5]/[O:6][CH3:7].[BH-](OC(C)=O)(OC(C)=O)O[C:31](C)=O.[Na+].C=O.C(=O)(O)[O-].[Na+]>C(Cl)Cl>[CH3:1][O:2][C:3](=[O:28])/[C:4](/[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[CH2:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([N:22]([CH2:23][CH:24]([CH3:26])[CH3:25])[CH3:31])=[CH:18][C:17]=1[F:27])=[CH:5]/[O:6][CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 712FormaldehydeHCID 516892Sodium BicarbonateHCID 5049666Sodium triacetoxyborohydrideHCID 11617976HCID 11617976, 화합물

생성물 1

HCID 11596500HCID 11596500, 화합물수율 73%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

70 mg (0.18 mmol) of the compound obtained in Step 3 was dissolved in 1.5 ml of methylene chloride, and 57 mg (0.27 mmol) of NaBH(OAc)3 and 30 μl (0.40 mmol) of formaldehyde were added thereto. After stirring at room temperature for 22 hours, the reaction mixture was treated with a saturated sodium bicarbonate aqueous solution, and the water layer was separated and extracted twice with 10 ml of methylene chloride. The organic layers were combined, dried over anhydrous MgSO4, and concentrated under a reduced pressure. The residue was subjected to column chromatography using 20% ethyl acetate/hexane as an eluent to obtain 50 mg (yield 73%) of (E)-methyl-2-[2-((4-(N-isobutyl-N-methylamino)-2-fluorophenoxy)methyl)phenyl]-3-methoxyacrylate as an oil.

후처리

  1. customthe water layer was separated
  2. extractionextracted twice with 10 ml of methylene chloride
  3. dry with materialdried over anhydrous MgSO4
  4. concentrationconcentrated under a reduced pressure

출처 및 근거

ORD 기록
ord-0b08bc7eed9d4b8f89f1506c12b150a4
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879835B2

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