ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

HCID 86747712、化合物 → HCID 18957438、化合物

HRID 2379534
ノート
印刷プレビュー

反応式

HRID 2379534 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 86747712HCID 86747712、化合物

生成物 1

HCID 18957438HCID 18957438、化合物収率 45.6%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

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.

後処理

  1. customevaporated in vacuo
  2. additionThe 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
  • 出典と根拠

    ORDレコード
    ord-c681dda1a97c4bdeaf913a6fdcf90dbe
    出典データセット
    uspto-grants-1994_11
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US05362906

    反応ノート

    読み込み中…

    このページの内容参加物実験手順後処理出典と根拠反応ノート