Bromoacetic Acid → N-(5-Amino-1-carboxypentyl)iminodiacetic acid

HRID 2288120ノート

反応式

HRID 2288120 の反応式
Br[CH2:2][C:3]([OH:5])=[O:4].C(OC([NH:16][CH2:17][CH2:18][CH2:19][CH2:20][C@@H:21]([C:23]([OH:25])=[O:24])[NH2:22])=O)C1C=CC=CC=1>[OH-].[Na+]>[C:3]([CH2:2][N:22]([CH2:2][C:3]([OH:5])=[O:4])[C@H:21]([C:23]([OH:25])=[O:24])[CH2:20][CH2:19][CH2:18][CH2:17][NH2:16])([OH:5])=[O:4]

参加物

4

反応条件

温度
0 °C

実験手順

Bromacetic acid (28 g, 200 mmole) was dissolved in 100 ml of 2 M sodium hydroxide (NaOH) and cooled to 0° C. A solution of 28 g (100 mmole) of N'-benzyloxycarbonyl-L-lysine in 150 ml of 2 M NaOH was slowly added dropwise into the bromacetic acid solution while stirring in a 0° C. cooling bath. After 2 hours, the cooling bath was removed and the solution was stirred overnight at room temperature. The solution was then heated for two hours at 50° C. and 300 ml of 1 M hydrochloric acid (HCl) was added dropwise. The mixture was then cooled to room temperature allowing the N'-benzyloxycarbonyl-nitrilotriacetic acid (Z-NTA) to precipitate. The Z-NTA was collected by filtration and further purified by dissolving in 1 M NaOH, re-precipitating with the same amount of 1 M HCl and filtering. The dissolving and precipitating cycle was repeated twice.

後処理

  1. temperaturecooling bath
  2. customthe cooling bath was removed
  3. stirringthe solution was stirred overnight at room temperature
  4. temperatureThe solution was then heated for two hours at 50° C.
  5. addition300 ml of 1 M hydrochloric acid (HCl) was added dropwise
  6. temperatureThe mixture was then cooled to room temperature
  7. customto precipitate
  8. filtrationThe Z-NTA was collected by filtration
  9. customfurther purified
  10. dissolutionby dissolving in 1 M NaOH
  11. customre-precipitating with the same amount of 1 M HCl
  12. filtrationfiltering
  13. customThe dissolving and precipitating cycle

出典と根拠

ORDレコード
ord-98f200f7ee1649548d566e7161107936
出典データセット
uspto-grants-2000_07
特許番号
US06087452

反応ノート

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