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Methanol → 2-(Aminomethyl)-3,5-dichlorobenzenemethanol

HRID 1481333
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HRID 1481333 반응식
C([O:4][CH2:5][C:6]1[CH:11]=[C:10]([Cl:12])[CH:9]=[C:8]([Cl:13])[C:7]=1[C:14]#[N:15])(=O)C.O.CO>C1COCC1>[NH2:15][CH2:14][C:7]1[C:8]([Cl:13])=[CH:9][C:10]([Cl:12])=[CH:11][C:6]=1[CH2:5][OH:4]
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참가 물질

5

반응물 3

HCID 887MethanolHCID 962WaterHCID 897047603,5-Dichloro-2-cyanobenzyl acetate

생성물 1

HCID 897046962-(Aminomethyl)-3,5-dichlorobenzenemethanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
75 °C

실험 절차

To a solution of 3,5-dichloro-2-cyanobenzyl acetate (11.7 mmol) in 50 mL THF was added a solution of BH3 (50 mmol, 1M in THF). The reaction mixture was heated to 75° C. for 7 h and then cooled to 0° C. Water was added followed by MeOH and the mixture was concentrated. The residue was taken up in water and EtOAc, acidified with 1N HCl solution and extracted with DCM. The aqueous phase was then basified with 1M NaOH solution and extracted with DCM. The combined organic layers were dried over MgSO4 and concentrated in vacuo. Purification with CC using DCM/Et3N (99/1) to DCM/MeOH/Et3N (90/10/1) gives the desired compound as pinkish solid.

후처리

  1. temperaturecooled to 0° C
  2. concentrationthe mixture was concentrated
  3. extractionextracted with DCM
  4. extractionextracted with DCM
  5. dry with materialThe combined organic layers were dried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customPurification with CC

출처 및 근거

ORD 기록
ord-edb1037ba85146e69218818efdd5d281
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409917B2

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