تفاعل #1726674
ord-c571f5eb9e43484d96d111f6f13c1ec3
معادلة التفاعل
hydrogen
methyl benzoyl formate
(−) cinchonidine
→
(R)-methyl mandelate
المردود 99.7%
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1workup.ADDITIONwere mixed in an autoclave
- 2أخرىwas removed by filtration
- 3أخرىafter the reaction
- 4تركيزThe filtrate was concentrated
- 5أخرىthe residue was purified
الإجراء التجريبي
The cross-linked Ir—Pt cluster composition obtained in Example 13 (20.2 mg), methyl benzoyl formate (164.2 mg, 1.0 mmole), (−) cinchonidine (3.8 mg, 0.013 mmole) and toluene (5 ml) were mixed in an autoclave and agitated for five hours at room temperature in a hydrogen atmosphere at a pressure of 50 atmospheres. The cross linked Ir—Pt cluster composition was removed by filtration after the reaction. The filtrate was concentrated, and the residue was purified using PTLC to obtain (R)-methyl mandelate (165.6 mg, 99.7% yield). The asymmetric yield was 62.6% ee.