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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Barium Carbonate → HCID 86737305, 화합물

HRID 904575
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HRID 904575 반응식
Cl.[NH2:2][OH:3].C(=O)([O-])[O-].[Ba+2].[CH3:9][CH:10]1[CH:14]([C:15]([O:17][CH3:18])=[O:16])[C:13](=O)[CH:12]([CH3:20])[S:11]1>C(O)C>[OH:3][N:2]=[C:13]1[CH:12]([CH3:20])[S:11][CH:10]([CH3:9])[CH:14]1[C:15]([O:17][CH3:18])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10563Barium CarbonateHCID 443297Hydroxyamine hydrochlorideHCID 15526293HCID 15526293, 화합물

생성물 1

HCID 86737305HCID 86737305, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Hydroxylamine hydrochloride, 145 g (2.09 mol), and barium carbonate (J. T. Baker Chemical Company), 219.2 g (1.11 mol), are added to a solution of 89.3 g (0.474 mol) of tetrahydro-2,5-dimethyl-4-oxo-3-thiophenecarboxylic acid, methyl ester (Example C) in 1 L of absolute ethanol. The suspension is stirred and refluxed for sixteen hours, cooled, filtered through Supercell Hyflo® (Johns-Manville), the filtrate evaporated and the residue dissolved in 500 ml of diethyl ether. The diethyl ether solution is washed with 500 ml of water (2 times). The diethyl ether layer is separated, dried over anhydrous Na2SO4 and evaporated to give 83.7 g of tetrahydro-4-(hydroxyimino)-2,5-dimethyl-3-thiophenecarboxylic acid, methyl ester as an orange liquid.

후처리

  1. temperaturerefluxed for sixteen hours
  2. temperaturecooled
  3. filtrationfiltered through Supercell Hyflo® (Johns-Manville)
  4. customthe filtrate evaporated
  5. dissolutionthe residue dissolved in 500 ml of diethyl ether
  6. washThe diethyl ether solution is washed with 500 ml of water (2 times)
  7. customThe diethyl ether layer is separated
  8. dry with materialdried over anhydrous Na2SO4
  9. customevaporated

출처 및 근거

ORD 기록
ord-5640a57115d340dabdeeb84fec2a0566
출처 데이터셋
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04230707

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