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

Hydrochloric Acid → HCID 86635278, 화합물

HRID 1013515
노트
인쇄 미리보기

반응식

HRID 1013515 반응식
[N:1]1[CH:6]=[CH:5][C:4]([P:7](=[O:14])([O:11][CH2:12][CH3:13])[O:8][CH2:9][CH3:10])=[CH:3][CH:2]=1.[ClH:15]>CO.[OH-].[OH-].[Pd+2]>[ClH:15].[NH:1]1[CH2:2][CH2:3][CH:4]([P:7](=[O:14])([O:8][CH2:9][CH3:10])[O:11][CH2:12][CH3:13])[CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 3623756Diethyl pyridin-4-ylphosphonate

생성물 1

HCID 86635278HCID 86635278, 화합물

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 887Methanol용매

실험 절차

Diethyl pyridin-4-ylphosphonate (3.8 g, 17.66 mmol) and palladium hydroxide on carbon (1.240 g, 1.766 mmol) were taken up in MeOH (90 mL)/HCl (10 mL, 20.00 mmol). The suspension was agitated under H2 @ 40-50 psi for 7 days. The catalyst was removed by filtration and the filtrate concentrated in vacuo to give diethyl piperidin-4-ylphosphonate hydrochloride as a green gum. 1H NMR (DMSO-d6, 600 MHz) δ 9.26 (br s, 1H), 8.84 (br s, 1H), 3.96 (m, 4H), 3.20 (m, 2H), 2.80 (m, 2H), 2.10 (m, 1H), 1.84 (m, 2H), 1.68 (m, 2H), 1.19 (t, J=7.2 Hz, 6H). MS: cal'd 222 (MH+), exp 222 (MH+).

후처리

  1. customThe catalyst was removed by filtration
  2. concentrationthe filtrate concentrated in vacuo

출처 및 근거

ORD 기록
ord-3776f75d69e4483e8bbdc3c5bd12e788
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981874B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트