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Water → [4-(dimethylamino)phenyl][4-(9-H-thioxanthen-9-ylidene)-1-piperidinyl]methanone

HRID 223709
ノート
印刷プレビュー

反応式

HRID 223709 の反応式
[CH3:1][N:2]([CH3:12])[C:3]1[CH:11]=[CH:10][C:6]([C:7](Cl)=[O:8])=[CH:5][CH:4]=1.C(N(CC)CC)C.[CH:20]1[C:33]2[C:32](=[C:34]3[CH2:39][CH2:38][NH:37][CH2:36][CH2:35]3)[C:31]3[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=3)[S:25][C:24]=2[CH:23]=[CH:22][CH:21]=1.O>C(Cl)Cl>[CH3:1][N:2]([CH3:12])[C:3]1[CH:11]=[CH:10][C:6]([C:7]([N:37]2[CH2:38][CH2:39][C:34](=[C:32]3[C:33]4[CH:20]=[CH:21][CH:22]=[CH:23][C:24]=4[S:25][C:26]4[C:31]3=[CH:30][CH:29]=[CH:28][CH:27]=4)[CH2:35][CH2:36]2)=[O:8])=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 8471TriethylamineHCID 44007824-(Dimethylamino)benzoyl chlorideHCID 130525974-(9H-thioxanthen-9-ylidene)piperidine

生成物 1

HCID 13052598[4-(dimethylamino)phenyl][4-(9-H-thioxanthen-9-ylidene)-1-piperidinyl]methanone収率 40.5%

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒
2 回

実験手順

To a magnetically stirred, ice-cooled solution of p-dimethylaminobenzoyl chloride (0.02 mole) and triethylamine (20 ml) in methylene chloride (300 ml) under an argon atmosphere was added dropwise a solution of 4-(9-thioxanthylidene)-piperidine (0.0133 mole) in methylene chloride (100 ml) over a twenty minute period. After stirring for 48 hours at room temperature, water (250 ml) was added and the mixture stirred for an additional 30 minutes. The layers were separated and the organic layer was washed with water (100 ml), 5% sodium hydroxide (2×200 ml) and water (250 ml), and then dried over sodium sulfate, filtered and stripped under reduced pressure to a dark orange oil. The product was purified by low pressure column chromatography using a 25×1000 mm column packed with 250 g. of silica gel absorbent and eluted with ethyl acetate to yield 2.3 grams of the product. Recrystallization from toluene yielded 2.1 g. of product, m.p. 178°-186° C. (decomp.)

後処理

  1. stirringAfter stirring for 48 hours at room temperature
  2. stirringthe mixture stirred for an additional 30 minutes
  3. customThe layers were separated
  4. washthe organic layer was washed with water (100 ml), 5% sodium hydroxide (2×200 ml) and water (250 ml)
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. customThe product was purified by low pressure column chromatography
  8. washof silica gel absorbent and eluted with ethyl acetate

出典と根拠

ORDレコード
ord-63934fa7f6f64dd2a9ac27d6c7738c10
出典データセット
uspto-grants-1982_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04356184

反応ノート

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