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Tetraethyl (1-phenoxypropylidene)-bisphosphonate → (1-Phenoxypropylidene)-bisphosphonic acid

HRID 569618
노트
인쇄 미리보기

반응식

HRID 569618 반응식
[O:1]([C:8]([P:19](=[O:26])([O:23]CC)[O:20]CC)([P:11](=[O:18])([O:15]CC)[O:12]CC)[CH2:9][CH3:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C[Si](C)(C)Br>[O:1]([C:8]([P:19](=[O:20])([OH:23])[OH:26])([P:11](=[O:12])([OH:15])[OH:18])[CH2:9][CH3:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 53742288Tetraethyl (1-phenoxypropylidene)-bisphosphonate

생성물 1

HCID 20147886(1-Phenoxypropylidene)-bisphosphonic acid

시약·촉매·용매 1

HCID 76113Bromotrimethylsilane용매

실험 절차

A solution of tetraethyl (1-phenoxypropylidene)-bisphosphonate (2.1 g) in trimethyl bromosilane (8 ml) was kept at room temperature overnight, followed by evaporation in vacuo. The residue was stirred overnight in absolute ethanol. Evaporation in vacuo gave the desired compound.

후처리

  1. customfollowed by evaporation in vacuo
  2. customEvaporation in vacuo

출처 및 근거

ORD 기록
ord-ce4bfa27ba54486e83aac61cf44faeef
출처 데이터셋
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04732998

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