Hydrochloric Acid → N-(Chloroacetyl)-2-methylalanine

HRID 1824339Notes

Reaction equation

HRID 1824339 reaction equation
[NH2:1][C:2]([CH3:7])([CH3:6])[C:3]([OH:5])=[O:4].[OH-].[Na+].[Cl:10][CH2:11][C:12](Cl)=[O:13].Cl>O>[Cl:10][CH2:11][C:12]([NH:1][C:2]([CH3:7])([CH3:6])[C:3]([OH:5])=[O:4])=[O:13]

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 6119Aminoisobutyric acidHCID 6577Chloroacetyl chlorideHCID 14798Sodium Hydroxide2×

Product 1

HCID 17605750N-(Chloroacetyl)-2-methylalanineYield 62.4%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent2×

Conditions

Temperature
5 °C

Procedure

To a stirring mixture of 2-aminoisobutyric acid (165.8 g; 1.61 mol), sodium hydroxide (64.4 g; 1.61 mol) and 800 ml water cooled to 5° C., was added chloroacetyl chloride (200 g; 1.77 mol) and then a solution of sodium hydroxide (70.8 g; 1.77 mol) in 143 ml water. The temperature was maintained between 5 to 10° C. during the additions. The reaction mixture was then allowed to warm to room temperature and the solution was acidified with 165 ml of concentrated aqueous HCl. The precipitated solid was filtered and dried under vacuum to afford 180.4 g (62%) of product.

Workup

  1. temperatureThe temperature was maintained between 5 to 10° C. during the additions
  2. temperatureto warm to room temperature
  3. filtrationThe precipitated solid was filtered
  4. customdried under vacuum

Sources & evidence

ORD record
ord-82d8830dbfb74e98a65859749327afaf
Source dataset
uspto-grants-2006_05
Patent number
US07041755B2

Reaction notes

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