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Triphenylphosphine → HCID 18940749、化合物

HRID 356072
ノート
印刷プレビュー

反応式

HRID 356072 の反応式
[Br:1]N1C(=O)CCC1=O.[C:9]([N:16]([CH2:21][CH3:22])[CH2:17][CH2:18][CH2:19]O)([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C(Cl)Cl>[C:9]([N:16]([CH2:17][CH2:18][CH2:19][Br:1])[CH2:21][CH3:22])([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10]
参加物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 11776TriphenylphosphineHCID 67184N-bromobutanimideHCID 23092014tert-Butyl ethyl3-hydroxypropylcarbamate

生成物 1

HCID 18940749HCID 18940749、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

11 g (0.0618 mol) of N-bromosuccinimide are added in the course of 5 minutes, with stirring, to a solution, which has been cooled to 0° C., of 10.49 g (0.0516 mol) of 3-(N-BOC-ethylamino)-1-propanol and 16.23 g (0.0619 mol) of triphenylphosphine in 160 ml of methylene chloride. The reaction mixture is stirred for a further 30 minutes at 0°-20° C. and is then concentrated by evaporation in vacuo. The dark-colored oily residue is stirred with 200 ml of hexane, whereupon a brown precipitate forms. After filtration and concentration of the filtrate by evaporation in vacuo, the title compound is obtained in the form of an oil, Rf value=0.71 (silica gel/tert-butyl methyl ether).

後処理

  1. stirringThe reaction mixture is stirred for a further 30 minutes at 0°-20° C.
  2. concentrationis then concentrated by evaporation in vacuo
  3. stirringThe dark-colored oily residue is stirred with 200 ml of hexane, whereupon a brown precipitate forms
  4. filtrationAfter filtration and concentration of the filtrate
  5. customby evaporation in vacuo

出典と根拠

ORDレコード
ord-cbec98ad126d4d1299de25392abf95c1
出典データセット
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05834486

反応ノート

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