2,3-Dichloropropene → HCID 21875394, 화합물

HRID 1441806노트

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HRID 1441806 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[SH:11].[Cl:12][C:13]([CH2:15]Cl)=[CH2:14].C([O-])([O-])=O.[K+].[K+].CCOC(C)=O>CN(C=O)C.O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11][CH2:15][C:13]([Cl:12])=[CH2:14]

참가 물질

7

반응물 4

HCID 65652,3-DichloropropeneHCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 47130122-chloro-5-nitrobenzenethiol

생성물 1

HCID 21875394HCID 21875394, 화합물수율 89%

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

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온도
80 °C

실험 절차

A solution of 2-chloro-5-nitro-benzenethiol (1.0 g, 5.27 mmol, prepared in accordance with the procedure described by Still et al. Synth. Comm. 13, 1181 (1983)) in 15 mL DMF was treated with 2,3-dichloropropene (693 μL, 7.52 mmol) and K2CO3 (433 mg, 3.13 mmol). The mixture was heated at 80° C. for 2 h and then allowed to cool to rt. EtOAc (200 mL) and H2O (100 mL) were added. The organic phase was washed with H2O (2×250 mL), saturated aqueous NaCl (100 mL), dried over MgSO4, and concentrated in vacuo. The crude material was purified by flash column chromatography on silica gel eluting with 20% EtOAc in hexanes to give compound 260A (1.09 g, 89%) as an orange oil.

후처리

  1. temperatureto cool to rt
  2. washThe organic phase was washed with H2O (2×250 mL), saturated aqueous NaCl (100 mL)
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated in vacuo
  5. customThe crude material was purified by flash column chromatography on silica gel eluting with 20% EtOAc in hexanes

출처 및 근거

ORD 기록
ord-85ca8677847f47aeb437bb00412db972
출처 데이터셋
uspto-grants-2010_02
특허 번호
US07655689B2

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