Hydrochloric Acid → ethyl N-carbobenzoxy-N-(dichlorophosphonomethyl)glycinate

HRID 903006ノート

反応式

HRID 903006 の反応式
C(N(CP(O)(O)=O)CC(O)=O)C.[Cl:13]C(OCC1C=CC=CC=1)=O.C(=O)([O-])[O-].[Na+].[Na+].[ClH:30].[C:31]([N:41]([CH2:48][P:49]([OH:52])([OH:51])=[O:50])[CH2:42][C:43]([O:45][CH2:46][CH3:47])=[O:44])([O:33][CH2:34][C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1)=[O:32]>O>[C:31]([N:41]([CH2:48][P:49]([O:51][Cl:13])([O:52][Cl:30])=[O:50])[CH2:42][C:43]([O:45][CH2:46][CH3:47])=[O:44])([O:33][CH2:34][C:35]1[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=1)=[O:32]

参加物

7

実験手順

Ethyl N-phosphonomethylglycine (9.85 g., 0.05 mole) and benzyl chloroformate (9.4 g., 0.05 mole) were dissolved in 50 ml. of water and sodium carbonate (7.95 g., 0.075 mole) was added over a 1/2 hour period. The solution was stirred until all of the benzyl chloroformate had reacted. Concentrated hydrochloric acid (12.5 ml) was then added. Upon standing ethyl N-carbobenzoxy-N-phosphonomethylglycinate separated as an oil. The oil was then dried in a vacuum dessicator over phosphorus pentoxide at 0.55 torr. A 4 g. sample of the oil was dissolved in oxalyl chloride (20 ml) and stirred until gas evolution ceased. The mixture was concentrated in vacuo to yield ethyl N-carbobenzoxy-N-(dichlorophosphonomethyl)glycinate as a colorless oil. The oil is treated with an excess of oxalyl chloride to convert it to ethyl N-carbobenzoxy-N-phosphonomethylglycine dichloride which is then reacted with the appropriate thiol of the formula

後処理

  1. customhad reacted
  2. customseparated as an oil
  3. dry with materialThe oil was then dried in a vacuum dessicator over phosphorus pentoxide at 0.55 torr
  4. dissolutionsample of the oil was dissolved in oxalyl chloride (20 ml)
  5. concentrationThe mixture was concentrated in vacuo

出典と根拠

ORDレコード
ord-c93de37adc104491bf9b34584ba87a7a
出典データセット
uspto-grants-1980_10
特許番号
US04226611

反応ノート

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