Hydrochloric Acid → (3,5-Dichloro-6-fluoro-2-pyridyloxy) acetic acid
반응식
C([O:3][C:4](=[O:16])[CH2:5][O:6][C:7]1[C:12]([Cl:13])=[CH:11][C:10]([Cl:14])=[C:9]([F:15])[N:8]=1)C.C(O)C.[OH-].[Na+].Cl>O>[Cl:13][C:12]1[C:7]([O:6][CH2:5][C:4]([OH:16])=[O:3])=[N:8][C:9]([F:15])=[C:10]([Cl:14])[CH:11]=1참가 물질
실험 절차
A mixture of 17 grams (0.06 mole) of ethyl-(3,5-dichloro-6-fluoro-2-pyridyloxy)acetate in 90 milliliters of commercial grade ethanol and 2.8 grams of sodium hydroxide in 25 milliliters of water was refluxed for ~20 minutes. Thereafter 5.9 cubic centimeters of concentrated hydrochloric acid was added thereto and the mixture stirred and cooled for 15 minutes. The mixture was filtered to recover the solid which precipitated and the solid was extracted exhaustively with boiling hexane followed by extraction with a hexane-benzene mixture. After drying, the (3,5-dichloro-6fluoro-2-pyridyloxy) acetic acid product was recrystallized from hexane and was recovered in a yield of ~6 grams and melted at 140°-144° C. Upon analysis, the product was found to have carbon, hydrogen, chlorine and nitrogen contents of 36.04, 2.11, 29.28 and 5.64 percent, respectively, as compared with the theoretical contents of 35.03, 1.67, 29.54 and 5.83 percent, respectively, calculated for the above-named compound.
후처리
- temperaturewas refluxed for ~20 minutes
- temperaturecooled for 15 minutes
- filtrationThe mixture was filtered
- customto recover the solid which
- customprecipitated
- extractionthe solid was extracted exhaustively with boiling hexane
- extractionfollowed by extraction with a hexane-benzene mixture
- customAfter drying
- customthe (3,5-dichloro-6fluoro-2-pyridyloxy) acetic acid product was recrystallized from hexane
- customwas recovered in a yield of ~6 grams and melted at 140°-144° C
출처 및 근거
- ORD 기록
- ord-5e83fd4075fb4a71a685cc5c3fac85d2
- 출처 데이터셋
- uspto-grants-1979_12
- 특허 번호
- US04180395
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