反应 #75427

ord-a3c6958a412c4737b0184493e43e5a7a

反应方程式

[Na+].[OH-]
sodium hydroxide
Cl
hydrochloric acid
COC(=O)Cl
methyl chloroformate
N[C@H](Cc1ccccc1)C(=O)O
D-phenylalanine
[Na+].[OH-]
sodium hydroxide
COC(=O)N[C@H](Cc1ccccc1)C(=O)O
oil
收率 113.9%
COC(=O)N[C@H](Cc1ccccc1)C(=O)O
(R)-2-(Methoxycarbonylamino)-3-phenylpropanoic acid
收率 113.9%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONWhen the addition
  2. 2
    workup.ADDITIONwas also added dropwise
  3. 3
    萃取The acid was extracted twice with diethylether
  4. 4
    洗涤the extracts were washed with brine
  5. 5
    干燥dried (MgSO4)
  6. 6
    其他The solvent was removed under vacuum

实验过程

A solution of D-phenylalanine (25.00 g, 0.151 mol) and sodium hydroxide (6.05 g, 0.151 mol) in water (170 ml) and tetrahydrofuran (225 ml) was cooled to −15° C., and a solution of methyl chloroformate (18.6 g, 0.197 mol) in tetrahydrofuran (50 ml) was added dropwise. When the addition was ˜half complete, a solution of sodium hydroxide (9.10 g, 0.227 mol) in water (20 ml) was also added dropwise. When the additions were complete, the mixture was stirred at room temperature for an additional 2 hours and acid fixed with 10% hydrochloric acid. The acid was extracted twice with diethylether, and the extracts were washed with brine and dried (MgSO4). The solvent was removed under vacuum to leave a clear oil (38.38 g). HPLC 6.01 min (78.9%), 7.32 min (5.0%), 8.29 min (10.8%), 8.42 min (0.5%), 9.95 min (1.2%), 10.27 min (2.8%), 11.92 min (0.7%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE038452E1uspto-grants-2004_03