Dimethylformamide → HCID 131722221, 화합물
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[C:1]([C:4]1[CH:9]=[C:8]([Cl:10])[C:7](Cl)=[CH:6][C:5]=1C)(=[O:3])[CH3:2].[SH:13][CH2:14][C:15]([CH3:20])([CH3:19])[C:16]([OH:18])=[O:17].[CH3:21]N(C)C=O.C(=O)([O-])[O-].[K+].[K+]>O>[C:1]([C:4]1[CH:5]=[CH:6][C:7]([S:13][CH2:14][C:15]([CH3:20])([CH3:19])[C:16]([OH:18])=[O:17])=[C:8]([Cl:10])[C:9]=1[CH3:21])(=[O:3])[CH3:2]참가 물질
실험 절차
A 100-ml three-necked round-bottomed flask was charged with 2.98 g (14.65 mmol) of 2-acetyl-4,5-dichlorotoluene, 1.72 g (12.84 mmol) of 3-mercaptopivalic acid and 15 ml of N,N-dimethylformamide under nitrogen atmosphere. Then, 3.04 g (22.00 mmol) of potassium carbonate was added. The reaction mixture was heated at 100~110° C. for 6 hours under nitrogen atmosphere. The reaction mixture was allowed to cool to room temperature, and about 150 ml of water was added. The mixture was washed with chloroform twice, and an aqueous layer was neutralized and acidified with a 5 wt % hydrochloric acid aqueous solution. A precipitated gummy substance was extracted with ethyl acetate, and an organic layer was washed with a 1 wt % hydrochloric acid aqueous solution, with water and with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure to give 3.02 g (yield 78%) of 3-(4-acetyl-2-chloro-methylphenylthio)pivalic acid.
후처리
- temperatureThe reaction mixture was heated at 100~110° C. for 6 hours under nitrogen atmosphere
- washThe mixture was washed with chloroform twice
- extractionA precipitated gummy substance was extracted with ethyl acetate
- washan organic layer was washed with a 1 wt % hydrochloric acid aqueous solution, with water and with a saturated sodium chloride aqueous solution
- dry with materialdried over anhydrous sodium sulfate
- distillationThen, the solvent was distilled off under reduced pressure
출처 및 근거
- ORD 기록
- ord-e7d8c0759c874612adf70846e156c823
- 출처 데이터셋
- uspto-grants-2000_12
- 특허 번호
- US06159904
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