반응식
[OH:1][N:2]1[C:6](=[O:7])[CH2:5][CH2:4][C:3]1=[O:8].P(Cl)(OC1C=CC=CC=1)([O:11][C:12]1C=CC=C[CH:13]=1)=O.C(N(CC)CC)C.C(O)(=O)C>C(OCC)(=O)C>[C:6]1(=[O:7])[N:2]([O:1][C:12](=[O:11])[CH3:13])[C:3](=[O:8])[CH2:4][CH2:5]1참가 물질
실험 절차
1.27 g (0.011 mol) of N-hydroxysuccinimide were initially introduced into 10 ml of ethyl acetate, a solution of 3.22 g (0.012 mol) of diphenyl chlorophosphate in 10 ml of ethyl acetate was added and then a solution of 2.53 g (0.025 mol) of triethylamine in 10 ml of ethyl acetate was added dropwise in the course of 10 minutes, the temperature rising to 41° C. A thick, white suspension resulted, which was treated with a solution of 0.6 g (0.01 mol) of acetic acid in 10 ml of ethyl acetate and heated at 45°-55° C. for 16 hours. After ending of the reaction, the solid was filtered off and washed with 2×3 ml of ethyl acetate. The combined filtrates were evaporated in vacuo and the semicrystalline residue which remained was washed by stirring with 20 ml of ethanol for 30 minutes. The white solid thus obtained was filtered off, washed with 2×3 ml of ethanol, sucked dry and then washed by stirring with 10 ml of isopropanol. After filtering off, washing with 2×2 ml of isopropanol and drying in vacuo, 1.1 g (70%) of white acetic acid succinimidyl ester were obtained.
후처리
- customrising to 41° C
- customA thick, white suspension resulted
- temperatureheated at 45°-55° C. for 16 hours
- customAfter ending of the reaction
- filtrationthe solid was filtered off
- washwashed with 2×3 ml of ethyl acetate
- customThe combined filtrates were evaporated in vacuo
- washthe semicrystalline residue which remained was washed
- customThe white solid thus obtained
- filtrationwas filtered off
- washwashed with 2×3 ml of ethanol
- customsucked dry
- washwashed
- stirringby stirring with 10 ml of isopropanol
- filtrationAfter filtering off
- washwashing with 2×2 ml of isopropanol
- customdrying in vacuo
출처 및 근거
- ORD 기록
- ord-46ef6b3fdcb74f75b3a22e357525e9cd
- 출처 데이터셋
- uspto-grants-1998_03
- 특허 번호
- US05734064
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