Bromotrimethylsilane → 4-(Bromomethyl)-1-methoxy-2-(3-methoxypropoxy)benzene

HRID 725641ノート

反応式

HRID 725641 の反応式
C[Si](C)(C)[Br:3].[CH3:6][O:7][C:8]1[CH:15]=[CH:14][C:11]([CH2:12]O)=[CH:10][C:9]=1[O:16][CH2:17][CH2:18][CH2:19][O:20][CH3:21]>C(Cl)(Cl)Cl>[CH3:6][O:7][C:8]1[CH:15]=[CH:14][C:11]([CH2:12][Br:3])=[CH:10][C:9]=1[O:16][CH2:17][CH2:18][CH2:19][O:20][CH3:21]

参加物

4

反応物 2

HCID 76113BromotrimethylsilaneHCID 451081634-Methoxy-3-(3-methoxypropoxy)benzenemethanol

生成物 1

HCID 115583294-(Bromomethyl)-1-methoxy-2-(3-methoxypropoxy)benzene

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

97 ml of trimethylbromosilane are added, with stirring at room temperature, to 113.1 g of 4-methoxy-3-(3-methoxypropyloxy)-benzyl alcohol in 1.31 liters of chloroform. After 10 minutes the solvent is evaporated off and the residue is immediately purified by means of FC (900 g of silica gel, eluant: ethyl acetate/hexane 1:3). The title compound is obtained: Rf (ethyl acetate/hexane=1:2)=0.34; m.p. 50°-51° C.

後処理

  1. customAfter 10 minutes the solvent is evaporated off
  2. customthe residue is immediately purified by means of FC (900 g of silica gel, eluant: ethyl acetate/hexane 1:3)

出典と根拠

ORDレコード
ord-14a306f66d2b4b0e9688f840a401cf20
出典データセット
uspto-grants-1998_01
特許番号
US05705658

反応ノート

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