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

HRID 1481341
ノート
印刷プレビュー

反応式

HRID 1481341 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

HCID 897048733-(Aminomethyl)-2-chlorobenzonitrile

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒
HCID 8857
Ethyl Acetate
溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-eee2ef8039454ec6938a4f4a85ae850f
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409917B2

反応ノート

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