反応式
Cl.[CH3:2][Si:3]([CH3:29])([CH3:28])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][NH:18][C:19]1[CH:27]=[CH:26][C:22]([C:23](Cl)=[O:24])=[CH:21][CH:20]=1.O1CCOCC1.[NH2:36][CH2:37][C:38]([O:40][CH2:41][CH3:42])=[O:39].C(Cl)Cl>CN(C)C1C=CN=CC=1.C(N(CC)CC)C>[CH3:2][Si:3]([CH3:29])([CH3:28])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][NH:18][C:19]1[CH:27]=[CH:26][C:22]([C:23](=[O:24])[NH:36][CH2:37][C:38]([O:40][CH2:41][CH3:42])=[O:39])=[CH:21][CH:20]=1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
A solution of 20 g. 4-[14-(trimethylsilyl)tetradecylamino]benzoyl chloride hydrochloride in 100 ml. dioxane is added to 4.9 g. freshly prepared ethyl glycinate in 300 ml. of methylene chloride containing 1 g. of 4-(dimethylamino)pyridine and 10 ml. of triethylamine. After 16 hours at room temperature the reaction is refluxed for 2 hours, cooled and filtered. The mother liquor is extracted with water and 10% hydrochloric acid. The solution is dried and concentrated in vacuo to an amber liquid. A sample is chromatographed on silica, appropriate fractions are pooled and evaporated to yield a solid which is recrystallized to a white solid.
後処理
- temperaturecooled
- filtrationfiltered
- extractionThe mother liquor is extracted with water and 10% hydrochloric acid
- customThe solution is dried
- concentrationconcentrated in vacuo to an amber liquid
- customA sample is chromatographed on silica, appropriate fractions
- customevaporated
- customto yield a solid which
- customis recrystallized to a white solid
出典と根拠
- ORDレコード
- ord-6b5996995f4e4a588ac5b7b2229113ed
- 出典データセット
- uspto-grants-1987_06
- 特許番号
- US04670421
関連ノート
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