Basic information Safety Supplier Related

(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic Acid Methyl Ester

Basic information Safety Supplier Related

(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic Acid Methyl Ester Basic information

Product Name:
(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic Acid Methyl Ester
Synonyms:
  • 3-Benzofuranaceticacid,2,3-dihydro-6-hydroxy-,Methylester
  • SR03298A
  • Methyl 2-(5-hydroxy-2,3-dihydro-1-benzofuran-3-yl)acetate
  • METHYL 2-(6-HYDROXY-2,3-DIHYDROBENZOFURAN-3-YL)ACETATE
  • methyl 2-(6-hydroxy-2,3-dihydro-1-benzofuran-3-yl)acetate
  • SR-03298A;SR 03298A;SR03298A
  • CS-1044
  • -Benzofuranaceticacid,2,3-dihydro-6-hydroxy-,Methylester
CAS:
805250-17-3
MF:
C11H12O4
MW:
208.21
Mol File:
805250-17-3.mol
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(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic Acid Methyl Ester Chemical Properties

Boiling point:
326.5±42.0℃ (760 Torr)
Density 
1.257±0.06 g/cm3 (20 ºC 760 Torr)
Flash point:
126.9±21.4℃
storage temp. 
Sealed in dry,Room Temperature
pka
9.77±0.40(Predicted)
Appearance
White to off-white Solid
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(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic Acid Methyl Ester Usage And Synthesis

Uses

(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic Acid Methyl Ester was used in the synthetic preparation of TAK-875 (T004915), a novel oral medication that has been developed to improve the secretion of insulin in a glucose-dependent manner, which has the potential to improve the control of blood sugar levels without the risk of hypoglycemia.

Synthesis

726174-52-3

805250-17-3

Methyl 2-(6-hydroxybenzofuran-3-yl)acetate (2 g, 9.71 mmol) was used as starting material and dissolved in methanol. A catalytic amount of palladium carbon (0.2 g) was added and three hydrogen substitutions were performed to exclude air. Subsequently, the reaction was stirred at room temperature for 24 h under hydrogen atmosphere. Upon completion of the reaction, the filtration was carried out using diatomaceous earth as a filter aid and the filter cake was washed with an appropriate amount of solvent. The filtrates were combined and the solvent was removed by distillation under reduced pressure to afford the off-white powdery solid product methyl 2,3-dihydro-6-hydroxy-3-coumarone acetate (1.93 g, 95% yield).

References

[1] Patent: CN105566267, 2016, A. Location in patent: Paragraph 0098-0101
[2] Patent: CN105566263, 2016, A. Location in patent: Paragraph 0087-0090
[3] Patent: CN105017242, 2018, B. Location in patent: Paragraph 0083-0086
[4] Patent: WO2008/1931, 2008, A2. Location in patent: Page/Page column 88
[5] Patent: WO2012/72691, 2012, A1. Location in patent: Page/Page column 51

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