Triethylamine → 3-Isopropoxyphenyl isothiocyanate

HRID 362599

反応式

HRID 362599 の反応式
[CH:1]([O:4][C:5]1[CH:6]=[C:7]([CH:9]=[CH:10][CH:11]=1)[NH2:8])([CH3:3])[CH3:2].[C:12](Cl)(Cl)=[S:13].C(N(CC)CC)C>C(Cl)(Cl)Cl>[CH:1]([O:4][C:5]1[CH:6]=[C:7]([N:8]=[C:12]=[S:13])[CH:9]=[CH:10][CH:11]=1)([CH3:3])[CH3:2]

参加物

5

実験手順

To a solution of 3-isopropoxy aniline (6.0 g, 40 mmol), in 150 mL of CHCl3 was added dropwise thiophosgene (2.81 mL, 44 mmol) at 0° C. After the addition of thiophosgene, triethylamine (7.0 mL, 48 mmol) was added slowly and the reaction mixture was stirred for 2 hours at room temperature. It was then concentrated and diluted with 200 mL of ethyl acetate. The triethylamine hydrochloride salt was filtered off and the filtrate was concentrated to yield crude 3-isopropoxyphenyl isothiocyanate. The crude 3-isopropoxyphenyl isothiocyanate was dissolved in 150 mL of acetic acid, and anthranilic acid (6.04 g, 44 mmol) was added. The resulting reaction mixture was refluxed for 16 hours and then cooled to room temperature. The white solid was separated which was filtered to yield 9.0 g of the title compound (72.1%), mp 288°-290° C.

後処理

  1. additionwas added slowly
  2. concentrationIt was then concentrated
  3. additiondiluted with 200 mL of ethyl acetate
  4. filtrationThe triethylamine hydrochloride salt was filtered off
  5. concentrationthe filtrate was concentrated

出典と根拠

ORDレコード
ord-9ee579bdb27b405799eb3b9881422f30
出典データセット
uspto-grants-1999_02
特許番号
US05869665

関連ノート

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