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Hydrochloric Acid → 3-Chloro-2,6-difluoroaniline

HRID 2367155
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HRID 2367155 반응식
[Cl:1][C:2]1[C:3]([F:17])=[C:4]([NH:9]C(=O)OC(C)(C)C)[C:5]([F:8])=[CH:6][CH:7]=1.Cl>CO.O1CCOCC1>[Cl:1][C:2]1[C:3]([F:17])=[C:4]([C:5]([F:8])=[CH:6][CH:7]=1)[NH2:9]
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참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 86083514tert-Butyl (3-chloro-2,6-difluorophenyl)carbamate

생성물 1

HCID 177507453-Chloro-2,6-difluoroaniline수율 92.2%

시약·촉매·용매 2

HCID 887Methanol용매HCID 312751,4-Dioxane용매

실험 절차

A solution of 1,1-dimethylethyl (3-chloro-2,6-difluorophenyl)carbamate (437 mg, 1.66 mmol) in methanol (2 mL) was treated with 4 N hydrochloric acid in dioxane (2 mL) and heated for 1 min with a heat gun. After cooling, the volatile materials were removed in vacuo. The resulting residue was taken up in ethyl acetate and washed with sodium bicarbonate (sat). The organic phase was dried over magnesium sulfate, filtered, and concentrated yielding 3-chloro-2,6-difluoroaniline as a white solid (250 mg, 1.53 mmol, 92%). MS (EI) for C6H4ClF2N: 164 (MH+).

후처리

  1. temperatureheated for 1 min with a heat gun
  2. temperatureAfter cooling
  3. customthe volatile materials were removed in vacuo
  4. washwashed with sodium bicarbonate (sat)
  5. dry with materialThe organic phase was dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-b33453b416334c2781d1b024ac9a0681
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08697737B2

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