Dimethylamine → 2-(2-Iodo-5-methoxyphenyl)-N,N-dimethylacetamide

HRID 4282

反応式

HRID 4282 の反応式
C(Cl)(=O)C(Cl)=O.[I:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[CH:10][C:9]=1[CH2:16][C:17]([OH:19])=O.[CH3:20][NH:21][CH3:22].C(Cl)Cl>C1(C)C=CC=CC=1.CN(C=O)C>[CH3:20][N:21]([CH3:22])[C:17](=[O:19])[CH2:16][C:9]1[CH:10]=[C:11]([O:14][CH3:15])[CH:12]=[CH:13][C:8]=1[I:7]

参加物

7

反応物 4

HCID 674DimethylamineHCID 6344DichloromethaneHCID 65578Oxalyl chlorideHCID 8200712-(2-Iodo-5-methoxyphenyl)acetic acid

生成物 1

HCID 140254972-(2-Iodo-5-methoxyphenyl)-N,N-dimethylacetamide

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒HCID 6228Dimethylformamide溶媒

実験手順

A 16.7 g (0.19 mole) sample of oxalyl chloride was added dropwise at 0° C. to a solution of 50.0 g (0.17 mole) of 2-iodo-5-methoxybenzeneacetic acid in 310 ml dry toluene and 31.7 ml of DMF. The mixture was allowed to warm to room temperature and stir for 16 hours. The solution was cooled to 0° C. and dimethylamine gas was admitted until the mixture was strongly basic. The mixture was allowed to warm to room temperature and stir for three hours and methylene chloride was added. The organic layer was washed with water, dilute hydrochloric acid, and sodium hydroxide. The organic layer was dried with MgSO4 and evaporated in vacuo to give 54.2 g of N,N-dimethyl-2-iodo-5-methoxybenzeneacetamide, mp 86°-89° C.

後処理

  1. temperatureThe solution was cooled to 0° C.
  2. temperatureto warm to room temperature
  3. stirringstir for three hours
  4. washThe organic layer was washed with water, dilute hydrochloric acid, and sodium hydroxide
  5. dry with materialThe organic layer was dried with MgSO4
  6. customevaporated in vacuo

出典と根拠

ORDレコード
ord-376b3b80298747838d4894a89b3c46a4
出典データセット
uspto-grants-1988_02
特許番号
US04725602

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