홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium Bicarbonate → 1-Bromo-3-methoxymethoxy-5-vinyl-benzene

HRID 457535
노트
인쇄 미리보기

반응식

HRID 457535 반응식
[Li][CH2:2]CCC.[Br:6][C:7]1[CH:8]=[C:9]([CH:12]=[C:13]([O:15][CH2:16][O:17][CH3:18])[CH:14]=1)[CH:10]=O.C([O-])(O)=O.[Na+]>CCOCC.[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C1COCC1>[Br:6][C:7]1[CH:8]=[C:9]([CH:10]=[CH2:2])[CH:12]=[C:13]([O:15][CH2:16][O:17][CH3:18])[CH:14]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 516892Sodium BicarbonateHCID 192615953-Bromo-5-methoxymethoxy-benzaldehydeHCID 178418339Butyllithium

생성물 1

HCID 184399631-Bromo-3-methoxymethoxy-5-vinyl-benzene수율 76%

시약·촉매·용매 3

HCID 74505Methyltriphenyliphosphonium bromide촉매
HCID 3283
Diethyl Ether
용매
HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
0 °C

실험 절차

A solution of n-BuLi (5.65 mL of a 1.6 M solution in Et2O, 9.04 mmol) was added dropwise to a solution of methyltriphenylphosphonium bromide (3.23 g, 9.05 mmol) in THF (15 mL) that was cooled to 0° C. The resulting yellow solution was stirred for 30 m, cooled to −78° C., and a solution of 3-bromo-5-methoxymethoxy-benzaldehyde (1.58 g, 6.46 mmol) in anhydrous THF (15 mL) was added dropwise. The mixture was slowly warmed to RT, stirred for 16 h, and then added to a saturated aqueous solution of NaHCO3 (60 mL). The layers were separated, and the aqueous layer was extracted with Et2O (2×50 mL). The combined organic layers were washed with brine (30 mL), and dried with anhydrous MgSO4. The volatile materials were evaporated, and the remaining oil was purified by flash chromatography on silica gel (0% to 3% EtOAc/hexanes) to provide 600 mg (76%) of 1-bromo-3-methoxymethoxy-5-vinyl-benzene (113c).

후처리

  1. temperaturecooled to −78° C.
  2. temperatureThe mixture was slowly warmed to RT
  3. stirringstirred for 16 h
  4. customThe layers were separated
  5. extractionthe aqueous layer was extracted with Et2O (2×50 mL)
  6. washThe combined organic layers were washed with brine (30 mL)
  7. dry with materialdried with anhydrous MgSO4
  8. customThe volatile materials were evaporated
  9. customthe remaining oil was purified by flash chromatography on silica gel (0% to 3% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-a95c43220bdd42249fec4cf5ecd5eace
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07189718B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트