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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-Hydroxybutyric Acid → Lactic acid hydroxybutyric acid

HRID 618419
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HRID 618419 반응식
[C:1]([OH:6])(=[O:5])[C@H:2]([CH3:4])[OH:3].[OH:7][CH:8]([CH2:12][CH3:13])[C:9]([OH:11])=[O:10]>>[C:1]([OH:6])(=[O:5])[CH:2]([CH3:4])[OH:3].[OH:7][CH:8]([CH2:12][CH3:13])[C:9]([OH:11])=[O:10]
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참가 물질

3

반응물 2

HCID 112662-Hydroxybutyric AcidHCID 107689L-Lactic Acid

생성물 1

HCID 86754496Lactic acid hydroxybutyric acid수율 69.7%

실험 절차

A 90 wt % aqueous solution of L-lactic acid (50 g) and 50 g of hydroxybutyric acid were put into a reaction vessel equipped with a stirrer and a nitrogen-introducing tube. After substitution of nitrogen gas was carried out three times, the mixture was concentrated at 120° C. for 5 hours with stirring in a stream of nitrogen to give 65 g of lactic acid-hydroxybutyric acid oligomer. To the obtained oligomer was added 1.3 g of Baylith 5A with which sodium elution (381 ppm) had been observed. Then, the temperature was raised to 200° C., and the pressure was reduced gradually to 20 mmHg over 30 minutes. The mixture was stirred at 195±5° C. for 3 hours. After the pressure was reduced gradually to 1 mmHg over 30 minutes, the mixture was stirred at 195±5° C. for 7 hours to give lactic acid-hydroxybutyric acid copolymer in the molten state. The product was cooled to room temperature to give 28.15 g of lactic acid-hydroxybutyric acid copolymer as a light brown solid. The weight-average molecular weight of this copolymer was 58,000.

후처리

  1. customequipped with a stirrer
  2. additiona nitrogen-introducing tube
  3. concentrationthe mixture was concentrated at 120° C. for 5 hours

출처 및 근거

ORD 기록
ord-50fea683f332435b8b1432198e15f57f
출처 데이터셋
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05952455

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