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Phosgene → 3-(3,5-Dichlorophenoxy)-1-pyrrolidinecarbonyl Chloride

HRID 464419
ノート
印刷プレビュー

反応式

HRID 464419 の反応式
[C:1]([Cl:4])(Cl)=[O:2].C([N:12]1[CH2:16][CH2:15][CH:14]([O:17][C:18]2[CH:23]=[C:22]([Cl:24])[CH:21]=[C:20]([Cl:25])[CH:19]=2)[CH2:13]1)C1C=CC=CC=1>C1C=CC=CC=1>[Cl:24][C:22]1[CH:23]=[C:18]([CH:19]=[C:20]([Cl:25])[CH:21]=1)[O:17][CH:14]1[CH2:15][CH2:16][N:12]([C:1]([Cl:4])=[O:2])[CH2:13]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6371PhosgeneHCID 202629731-Benzyl-3-(3,5-dichlorophenoxy)pyrrolidine

生成物 1

HCID 135342583-(3,5-Dichlorophenoxy)-1-pyrrolidinecarbonyl Chloride

試薬・触媒・溶媒 1

HCID 241Benzene溶媒2 回

反応条件

温度
5 °C

実験手順

To a stirred solution of 200 ml of 2 molar phosgene in benzene under nitrogen gas was added dropwise over a 3 hr period, a solution of 115 g (0.358 mole) of 1-benzyl-3-(3,5-dichlorophenoxy)pyrrolidine in 100 ml of benzene. The resulting solution was concentrated on a rotary evaporator to give an oil. The oil was triturated three times with boiling 30/60 petroleum ether, decanting each time. The oil residue solidified on cooling. The solid was taken up in benzene and the solution filtered, charcoaled and filtered. Crystalline product was obtained by adding ligroin and cooling to 5° C. in the amount of 92.7 g (87.9%), m.p. 105°-107° C. A purer 3 g sample, m.p. 106°-108° C. was obtained from the petroleum ether on standing.

後処理

  1. concentrationThe resulting solution was concentrated on a rotary evaporator
  2. customto give an oil
  3. customThe oil was triturated three times
  4. customdecanting each time
  5. temperatureon cooling
  6. filtrationthe solution filtered
  7. filtrationfiltered
  8. customCrystalline product was obtained

出典と根拠

ORDレコード
ord-263eb2f0571a44b783b4a7c21c91d3c1
出典データセット
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04547514

反応ノート

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