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Gamma-Butyrolactone → 1-Butanol, 4-(butylamino)-

HRID 1275995
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HRID 1275995 반응식
C(N)CCC.C1(=O)OCCC1.[CH2:12]([NH:16][C:17](=O)[CH2:18][CH2:19][CH2:20][OH:21])[CH2:13][CH2:14][CH3:15].CC(C[AlH]CC(C)C)C>C1(C)C=CC=CC=1>[CH2:12]([NH:16][CH2:17][CH2:18][CH2:19][CH2:20][OH:21])[CH2:13][CH2:14][CH3:15]
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참가 물질

6

반응물 4

HCID 7302Gamma-ButyrolactoneHCID 8007ButylamineHCID 14487Diisobutylaluminum hydrideHCID 13060238N-butyl-4-hydroxybutanamide

생성물 1

HCID 206691-Butanol, 4-(butylamino)-

시약·촉매·용매 1

HCID 1140Toluene용매2회

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온도
70 °C

실험 절차

A solution of 8.1 g (110 mmol) of n-butylamine and 8.6 g of butyrolactone in 50 ml toluene was allowed to reflux under nitrogen atmosphere for 50 hours. Volatile solvents were removed in vacuo. To a solution of 3.18 gm (20 mmol) of the resultant N-butyl-4-hydroxybutyramide in 50 ml of toluene were added 120 ml (120 mmol) DIBAL(25% W). The solution was heated with stirring at 70° C. for 18 hours. After cooling to 0° C., the reaction was quenched with methanol (1/3 amount of DIBAL solution was used) followed by addition of saturated solution of Rochelle's salt. The mixture was extracted twice with EtOAc; the organic extracts were washed with brine and dried over Na2SO4.

후처리

  1. temperatureto reflux under nitrogen atmosphere for 50 hours
  2. customVolatile solvents were removed in vacuo
  3. temperatureThe solution was heated
  4. temperatureAfter cooling to 0° C.
  5. customthe reaction was quenched with methanol (1/3 amount of DIBAL solution was used)
  6. additionfollowed by addition of saturated solution of Rochelle's salt
  7. extractionThe mixture was extracted twice with EtOAc
  8. washthe organic extracts were washed with brine
  9. dry with materialdried over Na2SO4

출처 및 근거

ORD 기록
ord-ea5441af70fb4d00ab2254db349eca3c
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06162927

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