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

Methanol → HCID 54116443, 화합물

HRID 1195635
노트
인쇄 미리보기

반응식

HRID 1195635 반응식
[CH3:1][C:2](=[CH2:12])[CH2:3][CH2:4][O:5][CH:6]1[CH2:11][CH2:10][CH2:9][CH2:8][O:7]1.[BH4-].[Na+].[CH3:15][OH:16]>[OH-].[Na+].[Hg]>[CH3:15][O:16][C:2]([CH3:1])([CH3:12])[CH2:3][CH2:4][O:5][CH:6]1[CH2:11][CH2:10][CH2:9][CH2:8][O:7]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 887MethanolHCID 4311764Sodium borohydrideHCID 122906552H-Pyran, tetrahydro-2-[(3-methyl-3-butenyl)oxy]-

생성물 1

HCID 54116443HCID 54116443, 화합물수율 93%

시약·촉매·용매 2

HCID 23931Mercury촉매HCID 14798Sodium Hydroxide용매2회

실험 절차

To 2-(3-methyl-3-butenyloxy)tetrahydropyran (150.0 g, 881.0 mmol) in methanol (600 ml) was added mercuric acetate (309 g, 969 mmol) and the mixture was stirred until it became homogeneous. To this solution was added 0.5N NaOH (500 ml) in one portion followed by dropwise addition of 0.5N NaBH4 in 0.5N NaOH (500 ml). The mixture is stirred until mercury metal congeals at the bottom of the flask. The solution is decanted into a separatory funnel and extracted with ether (3×300 ml). The combined ethereal extracts are dried (MgSO4) and concentrated to afford 166 g (93%) of 2-(3-methoxy-3-methylbutyloxy)tetrahydropyran as a colorless liquid.

후처리

  1. customThe solution is decanted into a separatory funnel
  2. extractionextracted with ether (3×300 ml)
  3. dry with materialThe combined ethereal extracts are dried (MgSO4)
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-0db9edb1f4f04f4ab51c23f8f722f250
출처 데이터셋
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05112595

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트