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

Calcium Carbonate → HCID 22648003, 화합물

HRID 394081
노트
인쇄 미리보기

반응식

HRID 394081 반응식
Br[CH2:2][C:3]1[C:8]([Br:9])=[CH:7][C:6]([N+:10]([O-:12])=[O:11])=[CH:5][C:4]=1[Br:13].C([O-])([O-])=[O:15].[Ca+2]>O1CCOCC1.O>[OH:15][CH2:2][C:3]1[C:8]([Br:9])=[CH:7][C:6]([N+:10]([O-:12])=[O:11])=[CH:5][C:4]=1[Br:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 10112Calcium CarbonateHCID 22648021HCID 22648021, 화합물

생성물 1

HCID 22648003HCID 22648003, 화합물

시약·촉매·용매 2

HCID 962Water용매2회HCID 312751,4-Dioxane용매

실험 절차

A mixture of 1-bromomethyl-2,6-dibromo-4-nitrobenzene (4.45 g, 1 eq.) and CaCO3 (5.7 g, 5 eq.) in 1,4-dioxane (20 mL) and water (20 mL) was heated to and maintained at reflux overnight. The mixture was cooled, poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrousmgSO4, filtered and concentrated. The product was purified by silica gel chromatography (eluted with 4:1 hexanes:ethyl acetate) to give 1-Hydroxymethyl-2,6-dibromo-4-nitrobenzene. 1H NMR (500 MHz, CDCl3) δ CHCl3: 2.28 (1H, broad t), 5.05(2H, m), 8.397(2H, s).

후처리

  1. temperaturewas heated to and
  2. temperaturemaintained
  3. temperatureat reflux overnight
  4. temperatureThe mixture was cooled
  5. extractionextracted with ethyl acetate
  6. washThe organic layer was washed with brine
  7. customdried over anhydrousmgSO4,
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe product was purified by silica gel chromatography (eluted with 4:1 hexanes:ethyl acetate)

출처 및 근거

ORD 기록
ord-0b20ce1b46394d309386f5b920be8c26
출처 데이터셋
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06809199B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트