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

Hydrochloric Acid → 3,4-dihydro-2,5-dimethyl-8-nitro-2H-1-benzopyran

HRID 637628
노트
인쇄 미리보기

반응식

HRID 637628 반응식
Br[CH:2]([CH3:16])[CH2:3][CH2:4][C:5]1[C:10]([CH3:11])=[CH:9][CH:8]=[C:7]([N+:12]([O-:14])=[O:13])[C:6]=1[OH:15].[H-].[Na+].Cl>CS(C)=O>[CH3:16][CH:2]1[CH2:3][CH2:4][C:5]2[C:10]([CH3:11])=[CH:9][CH:8]=[C:7]([N+:12]([O-:14])=[O:13])[C:6]=2[O:15]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 24758Sodium hydrideHCID 135602952-(3-Bromobutyl)-3-methyl-6-nitrophenol

생성물 1

HCID 135602963,4-dihydro-2,5-dimethyl-8-nitro-2H-1-benzopyran

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

40.5 g of 1C was added in portions over 20 minutes to a stirred mixture of 3.4 g of sodium hydride in 300 ml of DMSO at room temperature, and the resulting mixture was stirred for 18 hours at room temperature. The mixture was poured into ice water, made slightly acidic with concentrated hydrochloric acid and filtered. The solid was dried to give 3,4-dihydro-2,5-dimethyl-8-nitro-2H-1-benzopyran (1D) as a yellow solid, m.p.: 83°-85° C.

후처리

  1. filtrationfiltered
  2. customThe solid was dried

출처 및 근거

ORD 기록
ord-a75eae1efd71446e90da5a071a985273
출처 데이터셋
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04558040

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트