Acetone → (R)-3-(N-Isopropylamino)-5-methoxychroman

HRID 1684096

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HRID 1684096 반응식
[CH:1]([NH:4][CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][C:12]=2[O:15][CH3:16])[O:7][CH2:6]1)([CH3:3])[CH3:2].CC1C=CC(C(O[C@H](C(O)=O)[C@H](OC(C2C=CC(C)=CC=2)=O)C(O)=O)=O)=CC=1.C(O)C.CC(C)=O>CCOCC.[OH-].[K+]>[CH:1]([NH:4][C@@H:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][C:12]=2[O:15][CH3:16])[O:7][CH2:6]1)([CH3:3])[CH3:2]

참가 물질

6

반응물 4

HCID 180AcetoneHCID 702EthanolHCID 263211Ditoluoyltartaric acid, (+)-HCID 19028181N-isopropyl-5-methoxychroman-3-amine

생성물 1

HCID 10489181(R)-3-(N-Isopropylamino)-5-methoxychroman수율 32%

시약·촉매·용매 1

HCID 88018273KOH diethylether용매

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온도
20 °C

실험 절차

The racemic 3-(N-isopropylamino)-5-methoxychroman (IV; 54 g, 0.224 mol) was mixed with an equimolar amount of (+)-di-1,4-toluoyl-D-tartaric acid (98.6 g, 0.244 mol). The mixture was dissolved in boiling ethanol (170 mL)/acetone (70 mL). The salt started to crystallize in the hot solvent mixture but was not filtered off until the solvent had cooled down to room temperature (20° C). The salt was then recrystallized nine times from ethanol acetone (1:5) to give the pure diastereomeric salt. Yield: 35% (54 g) (99% e.e). MD: 166°-168° C. The free enantiomer as the base (R)-3-(N-isopropylamino)-5-methoxychroman was obtained by the extraction of the salt in ether/KOH (1M). Yield: 32%, 17.5 g,

후처리

  1. dissolutionThe mixture was dissolved
  2. customto crystallize in the hot solvent mixture
  3. filtrationwas not filtered off until the solvent
  4. customThe salt was then recrystallized nine times from ethanol acetone (1:5)
  5. customto give the pure diastereomeric salt
  6. custom166°-168° C

출처 및 근거

ORD 기록
ord-4f6541ad729246219f147f199a032e8c
출처 데이터셋
uspto-grants-1997_06
특허 번호
US05639772

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