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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Squaric acid → Squaric Acid Hydroxymethylperimidine

HRID 718477
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인쇄 미리보기

반응식

HRID 718477 반응식
[C:1]1([OH:8])[C:5](=[O:6])[C:3](=[O:4])[C:2]=1[OH:7].OC[CH2:11][C:12]1[NH:13][C:14]2[CH:15]=[CH:16][CH:17]=[C:18]3[C:24]=2[C:22]([N:23]=1)=[CH:21][CH:20]=[CH:19]3>C(O)CCC>[C:1]1([OH:8])[C:2](=[O:7])[C:3](=[O:4])[C:5]=1[OH:6].[OH:4][CH2:11][C:12]1[NH:13][C:14]2[CH:15]=[CH:16][CH:17]=[C:18]3[C:24]=2[C:22]([N:23]=1)=[CH:21][CH:20]=[CH:19]3
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 17913Squaric acid2회HCID 117903368Hydroxyethyl perimidine

생성물 1

HCID 131734170Squaric Acid Hydroxymethylperimidine

시약·촉매·용매 1

HCID 2631-Butanol용매

실험 절차

To a 100 ml round bottom flask equipped with Teflon coated stir magnetic and a condenser was charged 1 g squaric acid (MW=114) and 45 g butanol. The round bottom flask was placed in an 80° C. oil bath. After the squaric acid dissolved, 4.0 g of the hydroxyethyl perimidine was added, as shown in the reaction below. The reaction progress was monitored by uv-vis spectrum. The peak at about 812 nm grew and peak at 354 decreased. The reaction was stopped when the 812 nm peak was considered maximized.

후처리

  1. customwas placed in an 80° C.
  2. customas shown in the reaction below

출처 및 근거

ORD 기록
ord-119d6afa16aa4be2ae1f88ddd9f1e80b
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09193869B2

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