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Hydrochloric Acid → (R)-1-(4-Chloro-3,5-dimethyl-phenyl)-propylamine

HRID 1629733
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HRID 1629733 반응식
[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([C@H:9]([NH:12][S@@](C(C)(C)C)=O)[CH2:10][CH3:11])=[CH:4][C:3]=1[CH3:19].Cl>CO>[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([C@H:9]([NH2:12])[CH2:10][CH3:11])=[CH:4][C:3]=1[CH3:19]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 67346503(R)-2-Methyl-propane-2-sulfinic acid [(R)-1-(4-chloro-3,5-dimethyl-phenyl)-propyl]-amide

생성물 1

HCID 55278509(R)-1-(4-Chloro-3,5-dimethyl-phenyl)-propylamine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of intermediate INT 37 (3.4 g, 11.26 mmol) in MeOH (75 mL) was treated with HCl (4 M in dioxane, 5.63 mL, 22.53 mmol) and stirred overnight. After evaporation of the solvents, a white solid was obtained which was washed with Et2O. The solid was then dissolved in water, slightly acidified with 2 M HCl and washed with EtOAc. The aqueous layer was separated and the pH adjusted to about 11 using 2 M NaOH followed by extraction with Et2O (3×). The Et2O layers were combined, dried over sodium sulfate, filtered and concentrated.

후처리

  1. customAfter evaporation of the solvents
  2. customa white solid was obtained which
  3. washwas washed with Et2O
  4. dissolutionThe solid was then dissolved in water
  5. washwashed with EtOAc
  6. customThe aqueous layer was separated
  7. extractionfollowed by extraction with Et2O (3×)
  8. dry with materialdried over sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ae478501eebb4f68a7ff21c73d12850d
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08791100B2

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