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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dichloromethane → 2-Bromo-3-(3,4-dichloro-phenyl)-propionaldehyde

HRID 1971831
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HRID 1971831 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][CH2:10][CH:11]=[O:12])[CH:5]=[CH:6][C:7]=1[Cl:8].C(Cl)Cl.C[Si]([Br:20])(C)C.BrBr>O.O1CCOCC1>[Br:20][CH:10]([CH2:9][C:4]1[CH:5]=[CH:6][C:7]([Cl:8])=[C:2]([Cl:1])[CH:3]=1)[CH:11]=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 6344DichloromethaneHCID 24408BromineHCID 76113BromotrimethylsilaneHCID 234995723-(3,4-Dichlorophenyl)propanal

생성물 1

HCID 581268402-Bromo-3-(3,4-dichloro-phenyl)-propionaldehyde

시약·촉매·용매 2

HCID 962Water용매

실험 절차

To a solution of the product of example 37 (10 mmol, 2.0 g) in a mixed solvent of DCM (40 ml) with dioxane (4.0 ml) was added TMSBr (15 mmol, 2.3 g) at room temperature. After the mixture was kept at 25° C. for one hour, bromine (1.6 g, 10.0 mmol) was added. Another one hour later, the mixture was poured into water (50 ml) and extracted with DCM three times. The combined organic layers were washed with brine, dried and evaporated into dryness to give the crude title product, which was used directly in the next step reaction.

후처리

  1. extractionextracted with DCM three times
  2. washThe combined organic layers were washed with brine
  3. customdried
  4. customevaporated into dryness

출처 및 근거

ORD 기록
ord-35dcfee7547d485687e67748015325b2
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08431581B2

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 31275
1,4-Dioxane
용매