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1-Bromo-3-chloropropane → HCID 69418516, 화합물

HRID 1375034
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HRID 1375034 반응식
Cl.[CH3:2][O:3][CH2:4][C@H:5]1[O:10][CH2:9][CH2:8][NH:7][CH2:6]1.Br[CH2:12][CH2:13][CH2:14][Cl:15].C(=O)([O-])[O-].[K+].[K+].C(OCC)(=O)C>CN(C)C=O.O>[ClH:15].[Cl:15][CH2:14][CH2:13][CH2:12][N:7]1[CH2:8][CH2:9][O:10][C@H:5]([CH2:4][O:3][CH3:2])[CH2:6]1
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참가 물질

7

반응물 4

HCID 80061-Bromo-3-chloropropaneHCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 53338717(2S)-2-(methoxymethyl)morpholine hydrochloride

생성물 1

HCID 69418516HCID 69418516, 화합물

시약·촉매·용매 2

HCID 962Water용매
HCID 6228
Dimethylformamide
용매

실험 절차

A mixture of (2S)-2-(methoxymethyl)morpholine hydrochloride (0.5 g), 1-bromo-3-chloropropane (1.47 ml) and potassium carbonate (2.06 g) in N,N-dimethylformamide (6 ml) was stirred at room temperature for 1 hour. After ethyl acetate and water were added to the mixture, the organic layer was separated, washed with water twice, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using ethyl acetate as an eluent. The fractions containing the objective compound were collected and evaporated under reduced pressure. The resulting oil was treated with 4N hydrogen chloride in ethyl acetate to give (2S)-4-(3-chloropropyl)-2-(methoxymethyl)morpholine hydrochloride (0.44 g).

후처리

  1. customthe organic layer was separated
  2. washwashed with water twice
  3. dry with materialdried over magnesium sulfate
  4. customevaporated under reduced pressure
  5. customThe residue was purified by column chromatography on silica gel
  6. additionThe fractions containing the objective compound
  7. customwere collected
  8. customevaporated under reduced pressure
  9. additionThe resulting oil was treated with 4N hydrogen chloride in ethyl acetate

출처 및 근거

ORD 기록
ord-7757821035044b2699d788c96731d326
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07166598B2

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