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Chemical Structure| 26278-23-9

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Product Details of [ 26278-23-9 ]

CAS No. :26278-23-9
Formula : C11H10O3
M.W : 190.20
SMILES Code : O=C(OC)CC1=COC2=CC=CC=C12
MDL No. :MFCD24849771

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Application In Synthesis of [ 26278-23-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 26278-23-9 ]

[ 26278-23-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 26278-23-9 ]
  • [ 64175-51-5 ]
YieldReaction ConditionsOperation in experiment
93% Example 70: Intermediate 63--1-benzofuran-3-yl acetic acid [0457] To METHYL-L-BENZOFURAN-3-YL acetate (10.8 g, 56. 8 mmol) in absolute ethanol (350 ml) was added 2. 5N NAOH (32 ml, 79.5 mmol) and the reaction mixture brought to reflux. After 30min of reflux, the reaction mixture was cooled down to room temperature and concentrated. The red solid was dissolved in H20 and acidified with 2N HC1. The precipitate that formed was dissolved in ethyl acetate. The aqueous layer was separated and extracted with ethyl acetate (2X). The organic extracts were combined, treated with brine, dried over anhydrous magnesium sulfate, filtered and concentrated. Chromatography ( (4 : 1) CH2CL2-MEOH (1% NH40H) ) generated the L-BENZOFURAN-3-YL acetic acid ammonium salt. This salt was then converted back to the acid by extraction with 1N HC1 and CH2C12. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated to afford 9. 31 g (93%) of 1- benzofuran-3-yl acetic acid as a peach solid. The product was characterized BY 1HNMR
With hydrogenchloride; lithium hydroxide monohydrate; In tetrahydrofuran; methanol; diethyl ether; n-heptane; water; EXAMPLE 7 Benzofuran-3-yl-acetic acid A solution of Example 6 (6.23 g, 33 mmol) and lithium hydroxide monohydrate (1.45 g, 35 mmol) in tetrahydrofuran (50 mL), water (35 mL), and methanol (14 mL) was stirred for 6.5 hours at room temperature. Water (70 mL) was added, and the reaction mixture was acidified to pH 4 using 2 M HCl and extracted with dichloromethane (5*200 mL). The organics were dried (MgSO4) and the solvent removed in vacuo to give a brown solid. This was dissolved in diethyl ether, heptane was added, and the mixture was stirred overnight. Solvent was removed by syringe to give product as a pale brown solid, 27 mmol, 80%. 1 H NMR (400 MHz, CDCl3): delta7.64 (1H, s); 7.58-7.56 (1H, m); 7.50-7.48 (1H, m); 7.34-7.24 (2H, m); 3.76 (2H, s).
  • 2
  • [ 67-56-1 ]
  • [ 64175-51-5 ]
  • [ 26278-23-9 ]
YieldReaction ConditionsOperation in experiment
100% With thionyl chloride; at -10 - 20℃; for 0.5h; General procedure: 5 g of acid (1) was dissolved in 40 mL of MeOH and cooled to -10C then 6 mL (3 eq) of SOCI2 were added dropwise. Obtained reaction mixture was allowed to warm to r.t. and stirred for additional 30 mi Volatiles were removed at reduced pressure and resi5 due was partitioned between 50 mL of ethyl acetate 50 mL of saturated solution of NaHCO 3, water fraction was additionally extracted with 30 mL of ethyl acetate, combined organic fractions were washed with 40 mL of saturated solution of NaCI, dried with Na2SO4 and evaporated in vacuum to afford compound (2).
 

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