Water → 2-(2-Bromoethyl)naphthalene

HRID 370646

反応式

HRID 370646 の反応式
P(Br)(Br)[Br:2].[CH:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][C:6]=1[CH2:15][CH2:16]O.N1C=CC=CC=1.O>C(Cl)(Cl)Cl>[Br:2][CH2:16][CH2:15][C:6]1[CH:7]=[CH:8][C:9]2[C:14](=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:5]=1

参加物

6

実験手順

A solution of phosphorus tribromide (3.52 g, 0.013 mol) in chloroform (6.25 ml) was added dropwise at -10° to a stirred solution of 2-naphthalene-ethanol (4.3 g, 0.025 mol) in chloroform (20 ml), containing dry pyridine (0.13 ml, 0.0016 mol). Following the addition, the mixture was stirred at -10° for 2 h, and was then stood at ambient temperature overnight. Next day, the reaction mixture was poured into water (62.5 ml) and the organic layer was separated. The aqueous solution was then extracted with chloroform (3×6.25 ml), and the organic layer and chloroform extracts were combined and washed with sodium hydroxide solution (62.5 ml, 2M), and with water (62.5 ml). The chloroform solution was dried (MgSO4), and the chloroform was then evaporated under reduced pressure to afford 2-(2-bromoethyl)naphthalene which was used without further purification.

後処理

  1. additionthe addition
  2. waitwas then stood at ambient temperature overnight
  3. customthe organic layer was separated
  4. extractionThe aqueous solution was then extracted with chloroform (3×6.25 ml)
  5. washwashed with sodium hydroxide solution (62.5 ml, 2M)
  6. dry with materialThe chloroform solution was dried (MgSO4)
  7. customthe chloroform was then evaporated under reduced pressure

出典と根拠

ORDレコード
ord-e3d7de8d34b647abb7333a2253c428b9
出典データセット
uspto-grants-1985_07
特許番号
US04528195

関連ノート

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