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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → I2-Ionone

HRID 1285233
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HRID 1285233 반응식
[CH3:1][C:2]([CH3:14])=[CH:3][CH2:4][CH2:5]/[C:6](/[CH3:13])=[CH:7]/[CH:8]=[CH:9]/[C:10]([CH3:12])=[O:11].S(=O)(=O)(O)O.O>C(Cl)Cl>[CH3:13][C:6]1[CH2:5][CH2:4][CH2:3][C:2]([CH3:14])([CH3:1])[C:7]=1/[CH:8]=[CH:9]/[C:10]([CH3:12])=[O:11]
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참가 물질

5

반응물 3

HCID 962WaterHCID 1118Sulfuric AcidHCID 1757003Pseudoionone

생성물 1

HCID 638014I2-Ionone수율 97%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 600 g of a 96% pure pseudoionone in 1,200 ml of methylene chloride was introduced continuously in the course of 10 minutes, while stirring vigorously (800 rpm), through one of the two connections of the reactor, and 1,000 ml of a 96% strength sulfuric acid were fed in simultaneously through the other connection. The product, which was discharged at 42° C., was hydrolyzed in a downstream thin film reactor with 2,000 ml of water, the organic phase was separated off, washed neutral with 2% strength sodium carbonate solution and then with water and freed from solvent under reduced pressure, and the residue was then distilled under 0.2 mbar. 495 g of 97.0% pure β-ionone were obtained, corresponding to a yield of β-ionone of 83.3% of theory. In this case too, the residue produced was a resin which exhibited good flow.

후처리

  1. customwas discharged at 42° C.
  2. customthe organic phase was separated off
  3. washwashed neutral with 2% strength sodium carbonate solution
  4. distillationthe residue was then distilled under 0.2 mbar

출처 및 근거

ORD 기록
ord-cdc24693777c4f1db3afc431ab80a8c3
출처 데이터셋
uspto-grants-1986_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04565894

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