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

Phosphorus sulfide (P2S5) → 4-Thioacetamidophenethyl Acetate

HRID 369565
노트
인쇄 미리보기

반응식

HRID 369565 반응식
[C:1]([O:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][C:14](=O)[CH3:15])=[CH:9][CH:8]=1)(=[O:3])[CH3:2].P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:18]>C1(C)C=CC=CC=1>[C:1]([O:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][C:14](=[S:18])[CH3:15])=[CH:9][CH:8]=1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14817Phosphorus sulfide (P2S5)HCID 125713974-Acetamidophenethyl acetate

생성물 1

HCID 232822924-Thioacetamidophenethyl Acetate수율 142.3%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

4-Acetamidophenethyl acetate (10.0 g, 45.2 mmol) and phosphorus pentasulfide (10.0 g, 22.5 mmol) were suspended in toluene (200 ml). The suspension was refluxed for 40 min. After cooling the supernatant was decanted into a separatory funnel and washed with 50% aqueous Na2CO3 solution (70 ml) and then with water (70 ml). The organic toluene layer was dried over anhydrous sodium sulfate overnight. The dried toluene solution was concentrated to dryness to give a yellowish solid (7.6 g, 71%). This solid was used for next reaction without further purification.

후처리

  1. temperatureThe suspension was refluxed for 40 min
  2. temperatureAfter cooling the supernatant
  3. customwas decanted into a separatory funnel
  4. washwashed with 50% aqueous Na2CO3 solution (70 ml)
  5. dry with materialThe organic toluene layer was dried over anhydrous sodium sulfate overnight
  6. concentrationThe dried toluene solution was concentrated to dryness

출처 및 근거

ORD 기록
ord-f4daf685128d4de4bd28c30416207fa9
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06140051

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트