Formaldehyde → L-Pantothenic acid

HRID 565175

反応式

HRID 565175 の反応式
[C:1]([OH:15])(=[O:14])[CH2:2][CH2:3][NH:4][C:5](=[O:13])[C@@H:6]([C:8]([CH2:11][OH:12])([CH3:10])[CH3:9])[OH:7].CC1(C)C(O)C(=O)OC1.C=O.C(=O)C(C)C.[C-]#N>>[C:1]([OH:15])(=[O:14])[CH2:2][CH2:3][NH:4][C:5](=[O:13])[C@H:6]([C:8]([CH2:11][OH:12])([CH3:10])[CH3:9])[OH:7]

参加物

6

反応物 5

HCID 712FormaldehydeHCID 989(+-)-PantolactoneHCID 5975CyanideHCID 6561IsobutyraldehydeHCID 6613Pantothenic Acid

生成物 1

HCID 5748353L-Pantothenic acid

実験手順

Pantothenic acid can be prepared by chemical synthesis, or biotechnologically by the fermentation of suitable microorganisms in suitable nutrient solutions. In the chemical synthesis, DL-pantolactone is an important compound. It is prepared in a multi-stage process from formaldehyde, isobutyraldehyde and cyanide. In further process steps, the racemic mixture is separated, D-pantolactone is subjected to a condensation reaction with β-alanine, and D-pantothenic acid is obtained.

後処理

  1. customIn further process steps, the racemic mixture is separated
  2. customD-pantolactone is subjected to a condensation reaction with β-alanine

出典と根拠

ORDレコード
ord-f43f0c8e4a324914a5e057090eee669e
出典データセット
uspto-grants-2001_01
特許番号
US06171845B2

関連ノート

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