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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Butanol → 2-Methylpropyl 2-hydroxypropanoate

HRID 248612
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HRID 248612 반응식
[C:1]([O:6][CH2:7][CH2:8][CH2:9]C)(=[O:5])[CH:2]([CH3:4])[OH:3].[C:11](O)(=O)C(C)O.C(O)CCC>Cl.O.C(O)CCC>[C:1]([O:6][CH2:7][CH:8]([CH3:9])[CH3:11])(=[O:5])[CH:2]([CH3:4])[OH:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 2631-Butanol2회HCID 612Lactic AcidHCID 8738Butyl Lactate3회

생성물 1

HCID 928142-Methylpropyl 2-hydroxypropanoate

시약·촉매·용매 2

HCID 313Hydrochloric Acid촉매HCID 22253497Water butanol용매

실험 절차

The composition of matter of 1-butyl lactate is and its preparation are disclosed in Gabriel et al. U.S. Pat. No. 1,668,806 (1928). They prepared 1-butyl lactate by dehydrating 70% lactic acid with excess 1-butanol at 117° C., followed by addition of HCl catalyst, followed by refluxing and esterification with addition excess 1-butanol and drawing a 1-butanol water azeotrope overhead. Nakanishi and Tsuda (Japanese Patent JP 46/30176 [71/30176]) consider production of 1-butyl lactate by extraction of an acidified crude fermentation broth with 1-butanol, followed by esterification of the extract phase. BASF (EP 159-285) considers production of isobutyl lactate by extraction of an acidified crude fermentation broth with isobutanol, followed by esterification of the extract phase, which was then distilled in vacuum 80° C./25 mbar to give a purified isobutyl lactate.

후처리

  1. customits preparation
  2. customat 117° C.
  3. temperatureby refluxing
  4. extractionby extraction of
  5. extractionby extraction of
  6. distillationwas then distilled in vacuum 80° C./25 mbar

출처 및 근거

ORD 기록
ord-5a37d7d15a7943c58ecb95b9ab25a852
출처 데이터셋
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05210296

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