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Sulfamic Acid → HCID 57955825, 화합물

HRID 553233
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HRID 553233 반응식
[CH2:1]([O:3][C:4]([C:6]1[C:10]([CH3:11])=[C:9]([CH:12]=[O:13])[O:8][C:7]=1[CH3:14])=[O:5])[CH3:2].S(N)(=O)(=O)[OH:16].Cl([O-])=O.[Na+]>C(O)(=O)C.O>[CH3:11][C:10]1[C:6]([C:4]([O:3][CH2:1][CH3:2])=[O:5])=[C:7]([CH3:14])[O:8][C:9]=1[C:12]([OH:16])=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 5987Sulfamic AcidHCID 23668197Sodium ChloriteHCID 85793152HCID 85793152, 화합물

생성물 1

HCID 57955825HCID 57955825, 화합물

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매2회

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
온도
0 °C

실험 절차

2,4-Dimethyl-5-formylfuran-3-carboxylic acid ethyl ester (1.78 g, 9.1 mmol) reported in the references was dissolved in a mixture of acetic acid (32 ml) and water (8 ml). Amidosulfuric acid (1.19 g, 12.2 mmol) was added to the solution, and cooled to 0° C. in an ice bath. Sodium chlorite was added and stirred for 2 hours, and after addition of water to reaction mixture, precipitate was collected by filtration, thereby giving 3,5-dimethyl-4-ethoxycarbonylfuran-2-carboxylic acid (1.01 g, 52%) as a white solid.

후처리

  1. customto reaction mixture, precipitate
  2. filtrationwas collected by filtration

출처 및 근거

ORD 기록
ord-a048c47779724b14a5f6b0fc1d4b35eb
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07951956B2

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