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Thionyl Chloride → 2-(4-Fluorophenoxy)benzyl chloride

HRID 2049647
ノート
印刷プレビュー

反応式

HRID 2049647 の反応式
S(Cl)([Cl:3])=O.[F:5][C:6]1[CH:20]=[CH:19][C:9]([O:10][C:11]2[CH:18]=[CH:17][CH:16]=[CH:15][C:12]=2[CH2:13]O)=[CH:8][CH:7]=1.C(=O)(O)[O-].[Na+]>C1C=CC=CC=1>[F:5][C:6]1[CH:20]=[CH:19][C:9]([O:10][C:11]2[CH:18]=[CH:17][CH:16]=[CH:15][C:12]=2[CH2:13][Cl:3])=[CH:8][CH:7]=1
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 24386Thionyl ChlorideHCID 516892Sodium BicarbonateHCID 3700253HCID 3700253、化合物

生成物 1

HCID 203438272-(4-Fluorophenoxy)benzyl chloride

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

8.5 g of thionyl chloride are added dropwise over a 10 minutes span to a stirring mixture of 13.0 g of 2-(4-fluorophenoxy)benzyl alcohol in 80 ml of benzene at ambient temperature. After total addition, the reaction mixture is stirred for 16 hours before being carefully poured onto 350 ml of crushed ice containing 8 ml of sodium bicarbonate. The mixture is stirred until the ice melts. The layers separate and the benzene layer is successively washed twice with 40 ml portions of a half saturated sodium bicarbonate solution, washed twice with 40 ml portions of water, washed once with a 25 ml portion of a saturated sodium chloride solution, dried and rotary evaporated to provide a clear liquid. The liquid is distilled at 106°-109° C. and 0.16 mm to provide a clear colorless liquid of 2-(4-fluorophenoxy)benzyl chloride.

後処理

  1. additionAfter total addition
  2. customThe layers separate
  3. washthe benzene layer is successively washed twice with 40 ml portions of a half saturated sodium bicarbonate solution
  4. washwashed twice with 40 ml portions of water
  5. washwashed once with a 25 ml portion of a saturated sodium chloride solution
  6. customdried
  7. customrotary evaporated
  8. customto provide a clear liquid
  9. distillationThe liquid is distilled at 106°-109° C.

出典と根拠

ORDレコード
ord-c4d013f87d784d7dba26ac0afe834a9a
出典データセット
uspto-grants-1980_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04198418

反応ノート

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