Formaldehyde → 4-hydroxy-N-methylproline

HRID 259836

反応式

HRID 259836 の反応式
[OH:1][C@H:2]1[CH2:6][NH:5][C@H:4]([C:7]([OH:9])=[O:8])[CH2:3]1.[CH2:10]=O>O.[Pd]>[CH3:10][N:5]1[CH2:6][C@H:2]([OH:1])[CH2:3][C@H:4]1[C:7]([OH:9])=[O:8]

参加物

5

反応物 2

HCID 712FormaldehydeHCID 5810L-Hydroxyproline

生成物 1

HCID 117687004-hydroxy-N-methylproline収率 98.3%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 962Water溶媒

実験手順

To 40 g (305 mmol) of trans-4-hydroxy-L-proline in 80 ml of water was added 80 ml of 30% aqueous formaldehyde solution and 7.0 g of 5% palladium on carbon catalyst (50% wet), and the mixture was hydrogenated at 50 psig using a Parr Shaker. After 24 hours, the catalyst was recovered by filtration over diatomaceous earth and the filtrate evaporated under reduced pressure to provide 43.5 g (98.3%) of title product; mp 140°-142° C. (decomposition); 1H-NMR (D2O): 4.65 (m, 1H), 4.20 (dd, 1H), 3.97 (dd, 1H), 3.2 (dm, 1H), 2.50 (m, 1H), 2.25 (m, 1H); [alpha]D =-54.8° (c=1.18, H2O).

後処理

  1. filtrationthe catalyst was recovered by filtration over diatomaceous earth
  2. customthe filtrate evaporated under reduced pressure

出典と根拠

ORDレコード
ord-b7fa990d4d8744399d7c1f3c3e3217fe
出典データセット
uspto-grants-1996_06
特許番号
US05523413

関連ノート

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