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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Propanoic acid, 2-bromo-2-methyl-, ethyl ester → 2-Amino-5,5-dimethyl-thiazol-4-one

HRID 355194
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HRID 355194 반응식
[NH2:1][C:2]([NH2:4])=[S:3].Br[C:6]([CH3:13])([CH3:12])[C:7](OCC)=[O:8]>C(O)C>[CH3:12][C:6]1([CH3:13])[S:3][C:2](=[NH:4])[NH:1][C:7]1=[O:8]
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참가 물질

4

반응물 2

HCID 11745Propanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 2723790Thiourea2회

생성물 1

HCID 1377015472-Amino-5,5-dimethyl-thiazol-4-one

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A suspension of thiourea (19.0 g, 0.25 mole) in 150 ml of ethanol was heated under reflux until all of the thiourea had dissolved. Ethyl 2-bromo-isobutyrate (49.0 g, 0.25 mole) was then added over 10 minutes to the refluxing solution, after which time the solution was heated under reflux for six hours then allowed to stir at ambient temperature 36 hours. The solution was concentrated to dryness and the residue treated with water, then with aqueous NaHCO3 to adjust the pH to 7.0. The precipitated solid was collected by filtration, washed with water and dried to yield 5,5-dimethyl-2-iminothiazolidin-4-one: mp 252°-254° C.; 15.0 g (0.12 mole, 47%). Structure was confirmed by IR and NMR.

후처리

  1. temperaturewas heated
  2. dissolutionhad dissolved
  3. temperatureafter which time the solution was heated
  4. temperatureunder reflux for six hours
  5. concentrationThe solution was concentrated to dryness
  6. additionthe residue treated with water
  7. filtrationThe precipitated solid was collected by filtration
  8. washwashed with water
  9. customdried

출처 및 근거

ORD 기록
ord-80212aeb42cb417da650a65c5c639c4b
출처 데이터셋
uspto-grants-1983_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04378357

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