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Hydrochloric Acid → L-Cysteine hydrochloride monohydrate

HRID 416677
ノート
印刷プレビュー

反応式

HRID 416677 の反応式
[ClH:1].[NH2:2][C@H:3]([C:6]([OH:8])=[O:7])[CH2:4][SH:5]>>[OH2:7].[ClH:1].[NH2:2][C@H:3]([C:6]([OH:8])=[O:7])[CH2:4][SH:5]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 313Hydrochloric AcidHCID 5862L-(+)-Cysteine2 回

生成物 1

HCID 23462L-Cysteine hydrochloride monohydrate

反応条件

温度
-10 °C

実験手順

500 ml of a purified L-cysteine-containing solution (eluate with 1N HCl) of example 7 or 9 (L-cysteine content=17 g/l) are concentrated to 25 ml. After adding concentrated HCl or introducing HCl gas, chlorides of inorganic alkali metal and alkaline earth metal ions and ammonium chloride may be crystallized, preferably at 20-60° C. After filtration, the L-cysteine-containing mother liquor is cooled to −10° C. and L-cysteine hydrochloride monohydrate crystallizes. Depending on the purity of the L-cysteine-containing solution used, L-cysteine hydrochloride monohydrate may be obtained in crystalline form in yields of >80% and purities of >90% from these solutions. It is possible to achieve purities of up to >98% by suitable control of the crystallization conditions, fractionated crystallization and/or recrystallization.

後処理

  1. concentrationare concentrated to 25 ml
  2. additionAfter adding concentrated HCl
  3. additionintroducing HCl gas, chlorides of inorganic alkali metal and alkaline earth metal ions and ammonium chloride
  4. custommay be crystallized, preferably at 20-60° C
  5. filtrationAfter filtration
  6. additionthe L-cysteine-containing mother liquor
  7. customL-cysteine hydrochloride monohydrate crystallizes
  8. additioncontaining solution

出典と根拠

ORDレコード
ord-25b21d06295f4ec6a1f72a2e675fa149
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08088949B2

反応ノート

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