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Isopropanol → (R)-N-methyl-3-hydroxy-3-phenylpropylamine hemioxalate salt

HRID 1724097
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HRID 1724097 반응식
I[CH2:2][CH2:3][C@H:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[OH:5].[I-].[Na+].C(O)(C)C.O.O.[C:20]([OH:25])(=[O:24])[C:21]([OH:23])=[O:22].[CH3:26][NH2:27]>O1CCCC1>[C:20]([OH:25])(=[O:24])[C:21]([OH:23])=[O:22].[CH3:26][NH:27][CH2:2][CH2:3][C@@H:4]([OH:5])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[CH3:26][NH:27][CH2:2][CH2:3][C@H:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[OH:5]
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참가 물질

7

반응물 5

HCID 3776IsopropanolHCID 5238Sodium IodideHCID 6329MethylamineHCID 61373Oxalic acid dihydrateHCID 14476875(R)-3-iodo-1-phenyl-1-propanol

생성물 1

HCID 131727265(R)-N-methyl-3-hydroxy-3-phenylpropylamine hemioxalate salt

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

실험 절차

A solution of (R)-3-iodo-1-phenylpropanol (5.0 g, 19 mmol) and catalytic amount of sodium iodide in tetrahydrofuran (20 mL) and 40% aqueous methylamine (40 mL) was stirred at room temperature for 5 hours. The reaction mixture was evaporated to 15 mL and the pH of the solution was adjusted to pH>12 via the addition of aqueous NaOH solution. The mixture was then twice extracted with toluene and the combined extracts were washed with brine. The toluene layer was evaporated to dryness and the residue dissolved in toluene (25 mL) and isopropanol (25 mL) and oxalic acid dihydrate (1.2 g, 9.5 mmol) was added and the mixture was stirred at room temperature for 2 hours. The resulting suspension was filtered and rinsed with toluene/isopropanol to give 3.0 g of (R)—N-methyl-3-hydroxy-3-phenylpropylamine hemioxalate salt as an off-white solid. The solid (2.9 g) was free based with sodium hydroxide solution and extracted with toluene. The extracts were washed with brine and then evaporated to dryness to give 2.2 g of (R)—N-methyl-3-hydroxy-3-phenylpropylamine as an off-white solid [α]D23=36° (c 1, CHCl3).

후처리

  1. customThe reaction mixture was evaporated to 15 mL
  2. additionthe pH of the solution was adjusted to pH>12 via the addition of aqueous NaOH solution
  3. extractionThe mixture was then twice extracted with toluene
  4. washthe combined extracts were washed with brine
  5. customThe toluene layer was evaporated to dryness
  6. dissolutionthe residue dissolved in toluene (25 mL)
  7. filtrationThe resulting suspension was filtered
  8. washrinsed with toluene/isopropanol

출처 및 근거

ORD 기록
ord-b6515616323c4f9cb2b2d34ac49876be
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07485754B2

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