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Nitric Acid → 3-Tert-butyl-2-hydroxy-5-nitrobenzaldehyde

HRID 2121281
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HRID 2121281 반응식
[C:1]([C:5]1[C:6]([OH:13])=[C:7]([CH:10]=[CH:11][CH:12]=1)[CH:8]=[O:9])([CH3:4])([CH3:3])[CH3:2].[N+:14]([O-])([OH:16])=[O:15]>C(O)(=O)C>[C:1]([C:5]1[C:6]([OH:13])=[C:7]([CH:10]=[C:11]([N+:14]([O-:16])=[O:15])[CH:12]=1)[CH:8]=[O:9])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 36786753-tert-Butyl-2-hydroxybenzaldehyde

생성물 1

HCID 125220373-Tert-butyl-2-hydroxy-5-nitrobenzaldehyde수율 64%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

5.0 g (28 mmol) of 3-tert-butyl-2-hydroxybenzaldehyde in 8 ml of glacial acetic acid were introduced into a 50 ml two-necked flask fitted with magnetic stirrer and dropping funnel, and 2.8 ml (68 mmol) of nitric acid were added at a temperature of below 5° C. The batch was subsequently stirred further at room temperature for one hour. The product was isolated by precipitation on ice and washed with water. After recyrstallization of the methanol, the product was dried. The yield was 64%.

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후처리

  1. customfitted with magnetic stirrer
  2. customThe product was isolated by precipitation on ice
  3. washwashed with water
  4. dry with materialAfter recyrstallization of the methanol, the product was dried

출처 및 근거

ORD 기록
ord-190f415a09f143debf5e88e4e9187211
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06695977B2

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