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

Sulfuric Acid → Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate

HRID 1877334
노트
인쇄 미리보기

반응식

HRID 1877334 반응식
[CH3:1][P:2](=[O:7])([O:5][CH3:6])[O:3][CH3:4].C([Li])CCC.[F:13][C:14]([F:24])([CH2:20][CH2:21][CH2:22][CH3:23])[C:15](OCC)=[O:16].OS(O)(=O)=O>O1CCCC1.CCCCC>[CH3:4][O:3][P:2]([CH2:1][C:15](=[O:16])[C:14]([F:24])([F:13])[CH2:20][CH2:21][CH2:22][CH3:23])(=[O:7])[O:5][CH3:6]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 1118Sulfuric AcidHCID 12958Dimethyl methylphosphonateHCID 10464909Ethyl 2,2-difluorohexanoateHCID 178418339Butyllithium

생성물 1

HCID 11118722Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate수율 44.1%

시약·촉매·용매 2

HCID 8003Pentane용매
HCID 8028Tetrahydrofuran용매

반응 조건

온도
-78 °C

실험 절차

A solution of dimethyl methylphosphonoate (6.5 g, 80 mmol, 2.2 equiv) in tetrahydrofuran (100 mL) was cooled to −78° C. and n-butyllithium (2.5 M in hexanes, 14 mL, 36 mmol, 1 equiv) was added dropwise. The solution was stirred at −78° C. for 30 min and ethyl 2,2-difluorohexanoate (6.5 g, 36 mmol, 1 equiv) was added dropwise. The solution was stirred at −78° C. for 1 h and warmed to 0° C. over 1 h. Pentane (100 mL) was added followed by the dropwise addition of 2M H2SO4 to pH=6. The aqueous layer was separated and extracted with pentane (3×15 mL). The organics were combined, dried over sodium sulfate, filtered, and concentrated to dryness under vacuum on a rotary evaporator. The crude oil was purified by column chromatography using methyl tert-butyl ether as eluant to afford 4.1 g of 26 as a yellow oil (44%).

후처리

  1. stirringThe solution was stirred at −78° C. for 1 h
  2. temperaturewarmed to 0° C. over 1 h
  3. customThe aqueous layer was separated
  4. extractionextracted with pentane (3×15 mL)
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated to dryness under vacuum on a rotary evaporator
  8. customThe crude oil was purified by column chromatography

출처 및 근거

ORD 기록
ord-5e49633d997d4f62b4de16338cca4132
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08309744B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트