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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dichloromethane → HCID 77230927, 화합물

HRID 1466078
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HRID 1466078 반응식
C(Cl)Cl.[Br:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12]([OH:14])=O)=[CH:7][C:6]=1[O:15][CH3:16].[C:17](Cl)(=O)[C:18](Cl)=O.[Cl-].[Cl-].[Cl-].[Al+3]>CN(C=O)C>[Br:4][C:5]1[CH:10]=[C:9]2[C:8](=[CH:7][C:6]=1[O:15][CH3:16])[CH2:11][C:12](=[O:14])[CH2:18][CH2:17]2
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참가 물질

6

반응물 4

HCID 6344DichloromethaneHCID 65578Oxalyl chlorideHCID 27529942-(4-Bromo-3-methoxyphenyl)acetic acidHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 77230927HCID 77230927, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a DCM solution of (4-Bromo-3-methoxyphenyl)acetic acid (900 mg, 3.67 mmol) was added oxalyl chloride (0.64 ml, 7.3 mmol) and a drop of DMF. The solution was allowed to stir at RT for 3 hours, at which point bubbling stopped. The volatiles were removed under vacuum, and the residue was redissolved in DCM. The solution was cooled to 0° C. To this solution was added aluminum trichloride (1.2 g, 9.2 mmol). After stirring the mixture for 15 minutes, ethylene was bubbled into the reaction. The reaction was poured into ice, extracted with DCM, washed with brine, and purified by MPLC. LC-MS (IE, m/z): 255 [M+1]+.

후처리

  1. custombubbling
  2. customThe volatiles were removed under vacuum
  3. dissolutionthe residue was redissolved in DCM
  4. temperatureThe solution was cooled to 0° C
  5. stirringAfter stirring the mixture for 15 minutes
  6. customethylene was bubbled into the reaction
  7. additionThe reaction was poured into ice
  8. extractionextracted with DCM
  9. washwashed with brine
  10. custompurified by MPLC

출처 및 근거

ORD 기록
ord-59fc9c353a2a4edda23d8ef403db896d
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08999990B2

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