Acetic Anhydride → 2-Acetamido-3-methoxypropanoic acid
반응식
[CH3:1][O:2][CH2:3][CH:4]([C:6]([OH:8])=[O:7])[NH2:5].[O:9]1CC[CH2:11][CH2:10]1.C(OC(=O)C)(=O)C>O>[C:10]([NH:5][CH:4]([C:6]([OH:8])=[O:7])[CH2:3][O:2][CH3:1])(=[O:9])[CH3:11]참가 물질
실험 절차
In a vessel, equipped with a mechanical stirrer, add at 20° C., 1.0 eq. of O-methyl-D,L-serine. Add 6 volumes of tetrahydrofuran and 0.65 volume of water. Add dropwise in 5 minutes 1.2 eq. of acetic anhydride. Stir mechanically the white suspension until complete conversion (HPLC monitoring, typical reaction time: 16 hours). At the end of the reaction the mixture becomes homogenous. Remove tetrahydrofuran as well as water azeotropically. Add toluene in order to remove completely water and acetic acid (KF and GC control). Crystallize the obtained crude solid in 6 volumes of acetone. Dry the wet solid at 40° C. under vacuum overnight. N-acetyl-O-methyl-D,L-serine (IX) is obtained as a white solid in 80% yield with a chemical purity of greater than 99% measured by HPLC.
후처리
- customIn a vessel, equipped with a mechanical stirrer
- additionadd at 20° C.
- customAt the end of the reaction the mixture
- customAdd toluene in order to remove completely water and acetic acid (KF and GC control)
- customCrystallize the
- customobtained crude solid in 6 volumes of acetone
- customDry the wet solid at 40° C. under vacuum overnight
출처 및 근거
- ORD 기록
- ord-69fa3b8424504c5c8701f8a51992736c
- 출처 데이터셋
- uspto-grants-2015_02
- 특허 번호
- US08946476B2
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