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Acetic Anhydride → Lactic Acid

HRID 1408
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HRID 1408 반응식
[CH3:1][CH2:2][CH2:3][CH2:4][CH:5]([OH:9])[C:6]([OH:8])=[O:7].C(O)(=O)[C@H](C)O.C(OC(=O)C)(=O)C>O>[C:6]([OH:8])(=[O:7])[CH:5]([CH3:4])[OH:9].[OH:9][CH:5]([CH2:4][CH2:3][CH2:2][CH3:1])[C:6]([OH:8])=[O:7]
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참가 물질

6

반응물 3

HCID 7918Acetic AnhydrideHCID 998242-Hydroxyhexanoic acidHCID 107689L-Lactic Acid

생성물 2

HCID 612Lactic AcidHCID 998242-Hydroxyhexanoic acid

시약·촉매·용매 1

HCID 962Water용매2회

반응 조건

온도
140 °C

실험 절차

DL-2-Hydroxycaproic acid (1.00 g, 0.0076 moles), and L-lactic acid (4.5 g of a nominally 85% solution in water; 0.043 moles) were placed in a reaction flask equipped with a distillation head and mechanical stirrer. The flask was heated at 110° C. for 6 hours under low vacuum (aspirator) while water was removed. The temperature was then raised to 140° C. for 6 hours. Acetic anhydride (5.16 g; 0.0506 moles) was added to the oligomer, followed by heating at 80° C. for 14 hours. Excess acetic anhydride and acetic acid were distilled off under low vacuum. Tetrahydrofuran/water (15 mL of 85/15; v/v) was added with stirring and heating at 60° C. for 0.5 hours. The bulk of the solvent was removed by vacuum distillation on a rotary evaporator. The resulting crude product was dissolved in chloroform (20 mL). The chloroform solution was washed twice with millipore water (5 mL) and then dried with MgSO4. The mixture was filtered through a "d" fritted glass funnel and the solvent distilled from the oligomer by rotary evaporation. Final traces of solvents were removed under high vacuum (0.4 mmHg) on a Kugelrohr apparatus at 120° C. to provide acetyl-oligo(D,L-2-hydroxycaproic-co-L-Lactic acid) with n=7.5 for lactic acid and 1.4 for hydroxycaproic acid, MN =763, and MW =1044.

후처리

  1. custom0.043 moles) were placed in a reaction flask
  2. customequipped with a distillation head and mechanical stirrer
  3. customwas removed
  4. temperatureby heating at 80° C. for 14 hours
  5. distillationExcess acetic anhydride and acetic acid were distilled off under low vacuum
  6. additionTetrahydrofuran/water (15 mL of 85/15; v/v) was added
  7. temperatureheating at 60° C. for 0.5 hours
  8. customThe bulk of the solvent was removed by vacuum distillation on a rotary evaporator
  9. dissolutionThe resulting crude product was dissolved in chloroform (20 mL)
  10. washThe chloroform solution was washed twice with millipore water (5 mL)
  11. dry with materialdried with MgSO4
  12. filtrationThe mixture was filtered through a "d" fritted glass funnel
  13. distillationthe solvent distilled from the oligomer by rotary evaporation
  14. customFinal traces of solvents were removed under high vacuum (0.4 mmHg) on a Kugelrohr apparatus at 120° C.

출처 및 근거

ORD 기록
ord-82348284bdb74ce681d8c47598cef413
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05725841

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