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Hydrochloric Acid → 3-(Aminomethyl)-2-chlorobenzonitrile

HRID 1481341
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HRID 1481341 반응식
Br[CH2:2][C:3]1[C:4]([Cl:11])=[C:5]([CH:8]=[CH:9][CH:10]=1)[C:6]#[N:7].[N-:12]=[N+]=[N-].[Na+].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.Cl>CN(C=O)C.CCOC(C)=O>[Cl:11][C:4]1[C:5]([C:6]#[N:7])=[CH:8][CH:9]=[CH:10][C:3]=1[CH2:2][NH2:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 11776TriphenylphosphineHCID 33557Sodium AzideHCID 571606383-(Bromomethyl)-2-chlorobenzonitrile

생성물 1

HCID 897048733-(Aminomethyl)-2-chlorobenzonitrile

시약·촉매·용매 2

HCID 6228Dimethylformamide용매
HCID 8857
Ethyl Acetate
용매

실험 절차

To a solution of 3-(bromomethyl)-2-chlorobenzonitrile (0.87 mmol) in 9 mL DMF was added NaN3 (1.3 mmol) and the resulting brown solution was stirred at RT for 20 min. The reaction mixture was diluted with EtOAc, washed twice with water and brine, dried over MgSO4 and concentrated in vacuo. The crude azide was redissolved in 4.3 mL THF and 0.1 mL water. Triphenylphosphine (1.04 mmol) was added and the mixture was stirred at RT overnight. The reaction mixture was acidified with 0.1N HCl solution until pH 3 and it was extracted 3 times with Et2O. The ageous phase was basified with 1M NaOH solution and extracted 3 times with DCM. The combined organic layers were dried over MgSO4 and concentrated in vacuo to give the desired product as yellowish oil.

후처리

  1. washwashed twice with water and brine
  2. dry with materialdried over MgSO4
  3. concentrationconcentrated in vacuo
  4. dissolutionThe crude azide was redissolved in 4.3 mL THF
  5. stirringthe mixture was stirred at RT overnight
  6. extractionwas extracted 3 times with Et2O
  7. extractionextracted 3 times with DCM
  8. dry with materialThe combined organic layers were dried over MgSO4
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-eee2ef8039454ec6938a4f4a85ae850f
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409917B2

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