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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 86747712, 화합물 → HCID 18957438, 화합물

HRID 2379534
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HRID 2379534 반응식
[CH3:1]/[C:2](/[CH2:16][CH2:17]/[CH:18]=[C:19](\[CH3:26])/[CH2:20][CH2:21][CH:22]=[C:23]([CH3:25])[CH3:24])=[CH:3]\[CH2:4][CH2:5][S:6][CH2:7][P:8](=[O:15])([O:12]CC)[O:9]CC>C1(C)C=CC=CC=1>[CH3:1]/[C:2](/[CH2:16][CH2:17]/[CH:18]=[C:19](\[CH3:26])/[CH2:20][CH2:21][CH:22]=[C:23]([CH3:25])[CH3:24])=[CH:3]\[CH2:4][CH2:5][S:6][CH2:7][P:8](=[O:9])([OH:12])[OH:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 86747712HCID 86747712, 화합물

생성물 1

HCID 18957438HCID 18957438, 화합물수율 45.6%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

Diethyl [(E,E)-4,8,12-trimethyl-3,7,11 -tridecatrienyl]thiomethylphosphonate (0.256 g, 0.636 mmol) was deprotected in a similar fashion as that described in Step 2 of Example 2. The reaction mixture was added toluene (3 mL), then evaporated in vacuo. This process was repeated two more times. The final residue was treated with diluted hydrochloride acid (0.1N) at 0° C., then extracted with ethylacetate. The extract was washed with water the three time (3×10 ML). After drying and filtration, filtrate was concentrated in vacuo to give the title compound (0.1 g, 0.29 mmol, 45%) as a gum.

후처리

  1. customevaporated in vacuo
  2. addition
The final residue was treated with diluted hydrochloride acid (0.1N) at 0° C.
  • extractionextracted with ethylacetate
  • washThe extract was washed with water the three time (3×10 ML)
  • customAfter drying
  • filtrationfiltration, filtrate
  • concentrationwas concentrated in vacuo
  • 출처 및 근거

    ORD 기록
    ord-c681dda1a97c4bdeaf913a6fdcf90dbe
    출처 데이터셋
    uspto-grants-1994_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05362906

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