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

HRID 648352
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HRID 648352 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
21 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-e5ae875c251a42b3a6e615ab84192a7b
출처 데이터셋
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04411904

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