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Chloroacetyl chloride → 1'-(Chloroacetyl)-spiro[isobenzofuran-1(3H),4'-piperidine]

HRID 1782044
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HRID 1782044 반응식
[NH:1]1[CH2:6][CH2:5][C:4]2([C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=3[CH2:8][O:7]2)[CH2:3][CH2:2]1.C(N(C(C)C)C(C)C)C.[Cl:24][CH2:25][C:26](Cl)=[O:27]>C1COCC1>[Cl:24][CH2:25][C:26]([N:1]1[CH2:6][CH2:5][C:4]2([C:10]3[C:9](=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH2:8][O:7]2)[CH2:3][CH2:2]1)=[O:27]
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참가 물질

5

반응물 3

HCID 6577Chloroacetyl chlorideHCID 81531DiisopropylethylamineHCID 104424983H-spiro[2-benzofuran-1,4'-piperidine]

생성물 1

HCID 187002141'-(Chloroacetyl)-spiro[isobenzofuran-1(3H),4'-piperidine]

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
20 °C

실험 절차

3H-spiro[2-benzofuran-1,4′-piperidine] (5 g, 26 mmol) was dissolved in THF (100 mL) and cooled in ice. Then N-ethyldiisopropylamine (4.94 mL, 29 mmol) and chloroacetyl chloride (2.31 mL, 29 mmol) were added. The mixture was stirred at 20° C. for 15 min. The solid was filtered off and washed with THF. The filtrate was evaporated to dryness and the residue was purified by flash chromatography on silica gel with heptane/AcOEt 70:30. One obtained light yellow crystals (6.5 g, 92%). MS: m/z=266 [M+H]+.

후처리

  1. temperaturecooled in ice
  2. filtrationThe solid was filtered off
  3. washwashed with THF
  4. customThe filtrate was evaporated to dryness
  5. customthe residue was purified by flash chromatography on silica gel with heptane/AcOEt 70:30

출처 및 근거

ORD 기록
ord-cd6b3608e24a4c67b34d1bea3eb3db73
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07498339B2

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