反应 #742275

ord-f8e857b323dc4f299eb3c868e4ea4e32

反应方程式

N[C@@H](C(=O)N[C@@H]1C(=O)N2C(C(=O)O)=C(Cl)CS[C@H]12)c1ccccc1
cefaclor
N
ammonia
N[C@@H](C(=O)N[C@@H]1C(=O)N2C(C(=O)O)=C(Cl)CS[C@H]12)c1ccccc1.O
cefaclor monohydrate

试剂

溶剂

反应条件

温度
10°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤The suspension was filtered through a glass
  2. 2
    过滤filter
  3. 3
    洗涤the wet cake was washed with 2×15 ml water and 2×15 ml acetone
  4. 4
    其他After drying

实验过程

A crystallisation reactor was filled with 10 g water. The above-mentioned acidic cefaclor solution was dosed into the crystallisation reactor in 30 minutes at 25° C. The pH was kept at 5.0 with ammonia. Subsequently, the suspension was stirred at 10° C. for another 30 min. The suspension was filtered through a glass filter and the wet cake was washed with 2×15 ml water and 2×15 ml acetone. After drying, 18.3 g cefaclor monohydrate was obtained (purity 99.6%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08071330B2uspto-grants-2011_12