反应 #1747878

ord-bb2d5d2490484481b1dcf91886502af2

反应方程式

O=C(Cl)CCl
chloroacetyl chloride
O=C([O-])O.[Na+]
Sodium hydrogen carbonate
O=C([O-])O.[Na+]
sodium hydrogen carbonate
O=C(Cl)CCl
chloroacetyl chloride
O
water
Cl.Cl.NC[C@H]1CN(Cc2ccc(Cl)c(Cl)c2)CCO1
(2S)-2-Aminomethyl-4-(3,4-dichlorobenzyl)morpholine dihydrochloride
O=C(CCl)NC[C@H]1CN(Cc2ccc(Cl)c(Cl)c2)CCO1
(2S)-N-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}chloroacetamide

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度the mixture was cooled on an ice bath
  2. 2
    workup.ADDITIONwas added dropwise over about 10 min
  3. 3
    温度while maintaining the inside temperature at 15° C. or below
  4. 4
    workup.ADDITIONAfter the completion of the dropwise addition
  5. 5
    workup.WAITAfter 1.5 hr
  6. 6
    workup.STIRRINGthe mixture was further stirred for 1.5 hr
  7. 7
    其他partitioned

实验过程

(2S)-2-Aminomethyl-4-(3,4-dichlorobenzyl)morpholine dihydrochloride (120 g) was dissolved in tert-butyl methyl ether (450 ml), water (450 ml) was added and the mixture was cooled on an ice bath. Sodium hydrogen carbonate (95.56 g) was gradually added and, after the addition, chloroacetyl chloride (29 ml) was added dropwise over about 10 min while maintaining the inside temperature at 15° C. or below. After the completion of the dropwise addition, the mixture was stirred at room temperature for 1.5 hr. After 1.5 hr, sodium hydrogen carbonate (3 g) and chloroacetyl chloride (2.7 ml) were successively added to the reaction mixture at room temperature, and the mixture was further stirred for 1.5 hr. The reaction mixture was stood still and partitioned, and the organic layer was obtained as a solution of (2S)-N-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}chloroacetamide in tert-butyl methyl ether.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08030303B2uspto-grants-2011_10