Dimethyl Sulfoxide → N-p-toluoyl valinaldehyde

HRID 1835252ノート

反応式

HRID 1835252 の反応式
CS(C)=O.C(Cl)(=O)C(Cl)=O.[C:11]1([CH3:26])[CH:16]=[CH:15][C:14]([C:17]([NH:19][C@H:20]([CH2:24][OH:25])[CH:21]([CH3:23])[CH3:22])=[O:18])=[CH:13][CH:12]=1.C(N(CC)CC)C>C(Cl)Cl.C(OCC)(=O)C>[C:11]1([CH3:26])[CH:12]=[CH:13][C:14]([C:17]([NH:19][C@H:20]([CH:24]=[O:25])[CH:21]([CH3:23])[CH3:22])=[O:18])=[CH:15][CH:16]=1

参加物

7

反応物 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 18346087N-p-toluoyl valinol

生成物 1

HCID 53763109N-p-toluoyl valinaldehyde収率 56.6%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒2 回HCID 8857Ethyl Acetate溶媒

実験手順

Dimethylsulfoxide (2.2 ml, 31 mmol ) was slowly added via syringe to a stirred −78° C. solution of oxalyl chloride (15 ml, 171 mmol) in methylene chloride (35 ml) under inert. atmosphere. After 10 min., a solution of N-p-toluoyl valinol (6.0 g, 29 mmol) in methylene chloride (50 ml) was added and the stirring was continued for additional 15 min. Triethylamine was added (6 ml, 389 mmol) and the reaction was allowed to warm to ambient temperature. After 1.5 h, the reaction was diluted with 50% ethyl acetate in hexanes and washed with water and brine. Filtration through a pad of silica gel and subsequent solvent removal left a solid residue. Chromatography eluting with 20% ethyl acetate in hexanes, then 33% ethyl acetate in hexanes gave N-p-toluoyl valinaldehyde (3.6 g) as a solid, which was utilized in Step 6.

後処理

  1. waitthe stirring was continued for additional 15 min
  2. waitAfter 1.5 h
  3. washwashed with water and brine
  4. filtrationFiltration
  5. customthrough a pad of silica gel and subsequent solvent removal
  6. waitleft a solid residue
  7. washChromatography eluting with 20% ethyl acetate in hexanes

出典と根拠

ORDレコード
ord-221717eb54fb4f3586150e8d5903674c
出典データセット
uspto-grants-2004_08
特許番号
US06770650B2

反応ノート

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