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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(NE)-N-[1-(1-hydroxy-3,3-dimethyl-2,1-benzoxaborol-6-yl)ethylidene]hydroxylamine → 6-(1-aminoethyl)-3,3-dimethylbenzo[c][1,2]oxaborol-1(3H)-ol

HRID 1037127
노트
인쇄 미리보기

반응식

HRID 1037127 반응식
[OH:1][B:2]1[C:6]2[CH:7]=[C:8](/[C:11](=[N:13]/O)/[CH3:12])[CH:9]=[CH:10][C:5]=2[C:4]([CH3:16])([CH3:15])[O:3]1>CC(O)=O.[Zn]>[NH2:13][CH:11]([C:8]1[CH:9]=[CH:10][C:5]2[C:4]([CH3:15])([CH3:16])[O:3][B:2]([OH:1])[C:6]=2[CH:7]=1)[CH3:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 89573865(NE)-N-[1-(1-hydroxy-3,3-dimethyl-2,1-benzoxaborol-6-yl)ethylidene]hydroxylamine

생성물 1

HCID 866854916-(1-aminoethyl)-3,3-dimethylbenzo[c][1,2]oxaborol-1(3H)-ol

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

반응 조건

온도
40 °C

실험 절차

A mixture of crude compound (E)-1-(1-hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)ethanone oxime (0.93 mmol) and zinc dust (260 mg, 4.0 mmol) in AcOH (8 mL) was heated to 40° C. and stirred for 0.5 h. LC-MS showed SM disappeared. The reaction mixture was used for next reaction directly without being purified.

후처리

  1. customThe reaction mixture was used for next reaction directly
  2. customwithout being purified

출처 및 근거

ORD 기록
ord-a2d72ecd34f9447a8f968716fd359519
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08546357B2

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