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

Trimethyl orthoacetate → 1,3-Benzoxazol-4-ol

HRID 19391
노트
인쇄 미리보기

반응식

HRID 19391 반응식
Cl.[NH2:2][C:3]1[C:8]([OH:9])=[CH:7][CH:6]=[CH:5][C:4]=1[OH:10].[C:11](OC)(OC)(OC)C>S(=O)(=O)(O)O>[O:9]1[C:8]2=[CH:7][CH:6]=[CH:5][C:4]([OH:10])=[C:3]2[N:2]=[CH:11]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 15050Trimethyl orthoacetateHCID 4592471,3-Benzenediol, 2-amino-, hydrochloride (1:1)

생성물 1

HCID 137206971,3-Benzoxazol-4-ol수율 51%

시약·촉매·용매 1

HCID 1118Sulfuric Acid촉매

실험 절차

A mixture of 2-amino-benzene-1,3-diol hydrochloride (2.00 g, 12.4 mmol) and trimethyl orthoacetate (15 mL) was treated with concentrated sulfuric acid (5 drops) and the resulting mixture heated at reflux for 3 h, cooled and allowed to stand at room temperature overnight. The resulting mixture was concentrated in vacuo and the residue treated with ethyl acetate (200 mL), washed with water (200 mL) and brine (100 mL). The combined aqueous phases were extracted with ethyl acetate (200 mL) and the combined organic phases washed with brine and dried over sodium sulfate. The mixture was filtered and concentrated in vacuo which afforded benzooxazol-4-ol (0.94 g, 51%) as a yellow solid.

후처리

  1. temperaturethe resulting mixture heated
  2. temperatureat reflux for 3 h
  3. temperaturecooled
  4. concentrationThe resulting mixture was concentrated in vacuo
  5. additionthe residue treated with ethyl acetate (200 mL)
  6. washwashed with water (200 mL) and brine (100 mL)
  7. extractionThe combined aqueous phases were extracted with ethyl acetate (200 mL)
  8. washthe combined organic phases washed with brine
  9. dry with materialdried over sodium sulfate
  10. filtrationThe mixture was filtered
  11. concentrationconcentrated in vacuo which

출처 및 근거

ORD 기록
ord-e80020f93f3445a18bd2b839f88c261b
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07741327B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트