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

Triethylamine → HCID 15936310, 화합물

HRID 408960
노트
인쇄 미리보기

반응식

HRID 408960 반응식
[P:1]([Cl:5])(Cl)([Cl:3])=[O:2].[CH:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[CH:8][C:7]=1[OH:16].C(N(CC)CC)C>C(OCC)C>[P:1]([Cl:5])([Cl:3])(=[O:2])[O:16][C:7]1[CH:8]=[CH:9][C:10]2[C:15](=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 86632-NaphtholHCID 24813Phosphorus oxychloride

생성물 1

HCID 15936310HCID 15936310, 화합물수율 88%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

Phosphorus oxychloride (3.23 mL, 1 equiv) and β-naphthol (Aldrich, 5 g, 1 equiv) were stirred in anhydrous diethyl ether (25 mL). Anhydrous triethylamine was added (4.84 mL, 1 equiv) at −78° C. and the solution was allowed to warm to room temperature after 25 min. The triethylamine hydrochloride salt was filtered off and the solvent was removed under reduced pressure to give a clear pale yellow oil (7.95 g, 88%). (oil solidified in the freezer).

후처리

  1. filtrationThe triethylamine hydrochloride salt was filtered off
  2. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-0024b03ef7c34b46bbce420be62f29af
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08759318B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트