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Methanol → 3-[N,N-diphenylamino)-1-bromopropane

HRID 648352
ノート
印刷プレビュー

反応式

HRID 648352 の反応式
[Br:1][CH2:2][CH2:3][C:4]([N:6]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=O.B.CO>O1CCCC1>[C:7]1([N:6]([CH2:4][CH2:3][CH2:2][Br:1])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 887MethanolHCID 6331BoraneHCID 127638613-bromo-N,N-diphenyl propionamide

生成物 1

HCID 108273293-[N,N-diphenylamino)-1-bromopropane

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
21 °C

実験手順

A solution of 304 g. (1.00 moles) of 3-bromo-N,N-diphenyl propionamide in 800 ml. of tetrahydrofuran is stirred and maintained at -3° C. to -1° C. while adding 1.1 g. of a 1 molar solution of borane in tetrahydrofuran over a period of 15 minutes. The reaction is allowed to gradually warm to 21° C. over a period of about 1.75 hours and refluxed for a period of about 10 minutes. The reaction mixture is then treated dropwise with 50 ml. of methanol. After gas evolution ceases, solvent is removed under vacuum. The oily residue is dissolved in cyclohexane, washed with 20% caustic solution and then with water, dried and passed through a column of about 400 g. of silica gel, eluting with cyclohexane, to give 3-[N,N-diphenylamino]-1-bromopropane.

後処理

  1. temperaturemaintained at -3° C. to -1° C.
  2. additionwhile adding 1.1 g
  3. temperaturerefluxed for a period of about 10 minutes
  4. additionThe reaction mixture is then treated dropwise with 50 ml
  5. customAfter gas evolution ceases, solvent is removed under vacuum
  6. dissolutionThe oily residue is dissolved in cyclohexane
  7. washwashed with 20% caustic solution
  8. dry with materialwith water, dried
  9. washof silica gel, eluting with cyclohexane

出典と根拠

ORDレコード
ord-e5ae875c251a42b3a6e615ab84192a7b
出典データセット
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04411904

反応ノート

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