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Methanol → 2-[(-)-Isochroman-1-yl]-(+/-)-1-methylethylamine

HRID 368843
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HRID 368843 반응식
[CH:1]1([CH2:11][C:12](=O)[CH3:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][O:2]1.C([O-])(=O)C.[NH4+].CO.C([BH3-])#[N:23].[Na+]>C(O)(=O)C.C1COCC1>[CH:1]1([CH2:11][CH:12]([NH2:23])[CH3:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][O:2]1
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참가 물질

7

반응물 4

HCID 887MethanolHCID 517165Ammonium AcetateHCID 5003444Sodium cyanoborohydrideHCID 127770631-(Isochroman-1-yl)propan-2-one

생성물 1

HCID 232888322-[(-)-Isochroman-1-yl]-(+/-)-1-methylethylamine

시약·촉매·용매 2

HCID 176Acetic Acid용매
HCID 8028
Tetrahydrofuran
용매

실험 절차

A mixture of (-)-(isochroman-1-yl)acetone (LXXXIV, 0.73 g), ammonium acetate (1.48 g), methanol (2.5 ml), and THF (2.5 ml) is stirred for 25 min and then acetic acid (1.5 ml) and sodium cyanoborohydride (0.48 g) are added. After stirring for 2 hr, the mixture is concentrated and the residue is stirred with dichloromethane and sodium hydroxide (4N). The mixture is extracted with dichloromethane and washed with saline/sodium hydroxide (1N). The organic phase is separated and dried over sodium sulfate to give 2-[(-)-isochroman-1-yl]-(±)-1-methylethylamine.

후처리

  1. stirringAfter stirring for 2 hr
  2. concentrationthe mixture is concentrated
  3. stirringthe residue is stirred with dichloromethane and sodium hydroxide (4N)
  4. extractionThe mixture is extracted with dichloromethane
  5. washwashed with saline/sodium hydroxide (1N)
  6. customThe organic phase is separated
  7. dry with materialdried over sodium sulfate

출처 및 근거

ORD 기록
ord-0e687e9706ef40f6b1a61dab25d6fcb1
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06133446

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