Hydrochloric Acid → 2-Di-n-propylamino-8-chloro-1,2,3,4-tetrahydronaphthalene

HRID 274792

반응식

HRID 274792 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[CH2:10][C:9](=O)[CH2:8][CH2:7]2.[CH2:13]([NH:16][CH2:17][CH2:18][CH3:19])[CH2:14][CH3:15].[BH4-].[Na+].Cl>C1C=CC=CC=1.CO.C(O)C.C1(C)C=CC(S(O)(=O)=O)=CC=1.C(O)(=O)C.O>[CH2:13]([N:16]([CH2:17][CH2:18][CH3:19])[CH:9]1[CH2:8][CH2:7][C:6]2[C:11](=[C:2]([Cl:1])[CH:3]=[CH:4][CH:5]=2)[CH2:10]1)[CH2:14][CH3:15]

참가 물질

11

반응물 4

HCID 313Hydrochloric AcidHCID 8902DipropylamineHCID 4311764Sodium borohydrideHCID 46232698-Chloro-1,2,3,4-tetrahydronaphthalen-2-one

생성물 1

HCID 152333872-Di-n-propylamino-8-chloro-1,2,3,4-tetrahydronaphthalene수율 40%

시약·촉매·용매 6

HCID 6101p-Toluenesulfonic acid촉매HCID 176Acetic Acid용매HCID 241Benzene용매HCID 702Ethanol용매HCID 887Methanol용매HCID 962Water용매

실험 절차

To a solution of 8-chloro-2-tetralone (3.0 gm, 16.6 mMol) in benzene (25 mL) were added dipropylamine (3.35 mL, 33.2 mMol) and p-toluenesulfonic acid (100 mg), and the reaction mixture was heated at reflux for 4 hours with constant water removal (Dean-Stark trap). The reaction mixture was then cooled to room temperature, and the volatiles were removed in vacuo to give a dark viscous residue. To a solution of this crude material in methanol (30 mL) were added acetic acid (3 mL) followed by the dropwise addition of sodium borohydride (1.5 gm) in ethanol (60 mL) with cooling. The reaction mixture was stirred for 18 hours at room temperature. To this was then added hydrochloric acid (6M, 20 mL) and the mixture stirred 4 hours at room temperature. The volatiles were then removed in vacuo and the residue triturated with water. The aqueous phase was extracted once with diethyl ether, and the organic phase was discarded. The remaining aqueous phase was made basic with concentrated ammonium hydroxide and was then extracted well with dichloromethane. The organic extracts were combined, washed with saturated aqueous sodium chloride, dried over sodium sulfate and concentrated in vacuo to give an orange liquid. Purification by chromatography on basic alumina (Activity I, dichloromethane) gave a colorless liquid (1.75 gm, 40%). The hydrochloride salt was formed and recrystallized (ethanol/diethyl ether) to give a colorless, crystalline-solid (m.p.=159°-160° C.).

후처리

  1. temperaturethe reaction mixture was heated
  2. customthe volatiles were removed in vacuo
  3. customto give a dark viscous residue
  4. temperaturewith cooling
  5. customThe volatiles were then removed in vacuo
  6. customthe residue triturated with water
  7. extractionThe aqueous phase was extracted once with diethyl ether
  8. extractionwas then extracted well with dichloromethane
  9. washwashed with saturated aqueous sodium chloride
  10. dry with materialdried over sodium sulfate
  11. concentrationconcentrated in vacuo
  12. customto give an orange liquid
  13. customPurification by chromatography on basic alumina (Activity I, dichloromethane)

출처 및 근거

ORD 기록
ord-4ec84fe24cf141c6911214a221bdc060
출처 데이터셋
uspto-grants-1995_02
특허 번호
US05389687

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