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Imidazole → HCID 21180673, 화합물

HRID 1386763
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HRID 1386763 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH2:9][CH2:10][CH2:11]O)[CH:5]=[CH:6][C:7]=1[F:8].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N1C=CN=C1.[I:37]I>CCOCC.CCOCC.CC#N>[I:37][CH2:11][CH2:10][CH2:9][C:4]1[CH:5]=[CH:6][C:7]([F:8])=[C:2]([F:1])[CH:3]=1
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참가 물질

7

반응물 4

HCID 795ImidazoleHCID 807IodineHCID 11776TriphenylphosphineHCID 211806993-(3,4-Difluorophenyl)propan-1-ol

생성물 1

HCID 21180673HCID 21180673, 화합물수율 99.3%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매
HCID 21885917
Acetonitrile ether
용매

실험 절차

A solution of 2.00 g (11.6 mmol) of 3-(3,4difluorophenyl)propanol (from EXAMPLE 199, Step A), 3.96 g (15.1 mmol) of triphenylphosphine and 1.03 g (15.1 mmol) of imidazole in 2:1 v/v ether/CH3CN at 0° C. was treated with 4.10 g (16.3 mmol) of iodine. The resulting mixture was warmed to rt and stirred for 1 h. The mixture was diluted with 200 mL ether, and washed with sat'd Na2S2O3 (2×30 mL) and sat'd CuSO4 (30 mL). The organic phase was dried over MgSO4 and concentrated. The residue was partially dissolved in ether and filtered to remove triphenylphosphine oxide. The filtrate was concentrated. Flash chromatography on silica gel using 4:1 v/v hexanes/EtOAc afforded 3.25 g (99%) of the title compound.

후처리

  1. washwashed with sat'd Na2S2O3 (2×30 mL) and sat'd CuSO4 (30 mL)
  2. dry with materialThe organic phase was dried over MgSO4
  3. concentrationconcentrated
  4. dissolutionThe residue was partially dissolved in ether
  5. filtrationfiltered
  6. customto remove triphenylphosphine oxide
  7. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-a500c7d5fbb4460ebf6e1ccd11c1a3ae
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06265434B1

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