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

Sodium Hydroxide → HCID 54179458, 화합물

HRID 372560
노트
인쇄 미리보기

반응식

HRID 372560 반응식
[OH-].[Na+].Cl.[Cl:4][C:5]1[CH:18]=[CH:17][C:8]2[CH2:9][CH2:10][CH:11]([NH:15][CH3:16])[CH2:12][C:13](=[O:14])[C:7]=2[CH:6]=1>O>[Cl:4][C:5]1[CH:18]=[CH:17][C:8]2[CH2:9][CH2:10][CH:11]([NH:15][CH3:16])[CH2:12][CH:13]([OH:14])[C:7]=2[CH:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 131711106HCID 131711106, 화합물

생성물 1

HCID 54179458HCID 54179458, 화합물수율 92.7%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
10 °C

실험 절차

Sodium hydroxide solution was added to suspension of 4.6 g of the product of Step B in 100 ml of water cooled to 10° C and the mixture was extracted with methylene chloride. The extracts were dried and evaporated to dryness and the 4 g of oily residue were dissolved in 40 ml of ethanol and 4 ml of water. 2 g of sodium borohydride were added to the mixture at 20° C and the mixture was stirred for an hour. The mixture was evaporated to dryness and the residue was taken up in methylene chloride. The solution was washed with water, dried and evaporated to dryness. The residue was washed with isopropyl ether to obtain 3.7 g of 3-chloro-5ξ-hydroxy-7-methylamino-6,7,8,9-tetrahydro [5H] benzocycloheptene melting at 90° C.

후처리

  1. extractionthe mixture was extracted with methylene chloride
  2. customThe extracts were dried
  3. customevaporated to dryness
  4. dissolutionthe 4 g of oily residue were dissolved in 40 ml of ethanol
  5. addition2 g of sodium borohydride were added to the mixture at 20° C
  6. customThe mixture was evaporated to dryness
  7. washThe solution was washed with water
  8. customdried
  9. customevaporated to dryness
  10. washThe residue was washed with isopropyl ether

출처 및 근거

ORD 기록
ord-6088029bf0b246da8b337fcd30ae95d3
출처 데이터셋
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04091115

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트