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Propylamine → Propyl pentanesulfonamide

HRID 991296
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HRID 991296 반응식
[CH2:1]([S:6](Cl)(=[O:8])=[O:7])[CH2:2][CH2:3][CH2:4][CH3:5].[CH2:10](N)[CH2:11][CH3:12].C([N:16](C(C)C)C(C)C)C>C(Cl)Cl>[CH2:10]([CH:1]([S:6]([NH2:16])(=[O:8])=[O:7])[CH2:2][CH2:3][CH2:4][CH3:5])[CH2:11][CH3:12]
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참가 물질

5

반응물 3

HCID 7852PropylamineHCID 81531DiisopropylethylamineHCID 2375551-Pentanesulfonyl chloride

생성물 1

HCID 22322638Propyl pentanesulfonamide수율 95%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
0 °C

실험 절차

Pentane sulfonyl chloride (687 mg, 4.03 mmol) was dissolved in 5 mL CH2Cl2 and added to an ice-cooled solution of n-propylamine (0.40 mL, 4.82 mmol) and ethyldiisopropylamine (0.85 mL, 4.88 mmol) in 5 mL CH2Cl2 under a nitrogen atmosphere. The reaction was stirred at 0° C. for 30 min, then at 25° C. for 4 h. The solution was partitioned between 20 mL of 1.0 M aqeous NaHSO4 and 25 mL CH2Cl2. The organic phase was washed sequentially with 25 mL H2O and 25 mL brine, then dried (Na2SO4), filtered, and concentrated in vacuo to provide 739 mg (3.83 mmol, 95%) of the title compound as a white solid. TLC (25% EtOAc-hexane) Rf 0.23; 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, J=7 Hz, 3H), 0.97 (t, J=7 Hz, 3H), 1.28-1.50 (br m, 4H), 1.52-1.68 (m, 2H), 1.75-1.90 (br m, 2H), 2.98-3.06 (m, 2H), 3.08 (q, J=6 Hz, 2H), 4.10-4.23 (br m, 1H); MS (DCl/NH3) m/e 211 (M+NH4)+.

후처리

  1. waitat 25° C. for 4 h
  2. customThe solution was partitioned between 20 mL of 1.0 M aqeous NaHSO4 and 25 mL CH2Cl2
  3. washThe organic phase was washed sequentially with 25 mL H2O and 25 mL brine
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-cf9863b4a8914db0a40475345a7c47d4
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06462194B1

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