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Chemical Structure| 14282-64-5 Chemical Structure| 14282-64-5

Structure of 14282-64-5

Chemical Structure| 14282-64-5

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Product Details of [ 14282-64-5 ]

CAS No. :14282-64-5
Formula : C6H6O3S
M.W : 158.18
SMILES Code : O=C(C1=CC=C(CO)S1)O

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Application In Synthesis of [ 14282-64-5 ]

* 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 [ 14282-64-5 ]

[ 14282-64-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4565-31-5 ]
  • [ 14282-64-5 ]
YieldReaction ConditionsOperation in experiment
100% With sodium tetrahydroborate; In methanol; at 0 - 20℃; for 8h;Inert atmosphere; To a stirred solution of <strong>[4565-31-5]5-formyl-2-thiophenecarboxylic acid</strong> 16 (5.0 g, 32.0 mmol) in MeOH (160 mL) was added NaBH4 (1.82 g, 48.0 mmol) at 0C under nitrogen. The mixture was stirred at room temperature for 8 h. To the reaction mixture was added acetone and then evaporated. The residue was poured into 2 N HCl diluted with EtOAc. The aqueous layer was extracted with EtOAc. The combined organic extracts were washed with brine, dried over MgSO4, filtrated and then concentrated. The crude solid was washed with n-hexane/Et2O and filtrated to afford the title compound 17 as a light brown solid (quant.). 1H NMR (600 MHz, DMSO-d6): delta = 4.66 (s, 2H), 5.66 (br s, 1H), 6.99 (d, J = 3.8 Hz, 1H), 7.58 (d, J = 3.8 Hz, 1H), 12.90 (br s, 1H); 13C NMR (150 MHz, DMSO-d6): delta = 58.5, 124.3, 132.6, 133.0, 154.4, 163.0; HRMS-ESI m/z [M+H]+ calcd for C6H7O3S+:159.0110, found: 159.0112.
87% With methanol; sodium tetrahydroborate; at 20℃; for 4.5h;Inert atmosphere; Production Example 31-1 5-(Hydroxymethyl)thiophene-2-carboxylic acid Sodium borohydride (218 mg, 5.76 mmol) was added to a solution of commercially available <strong>[4565-31-5]5-formyl-2-thiophenecarboxylic acid</strong> (599 mg, 3.84 mmol) in methanol (19 mL), and the mixture was stiffed under nitrogen atmosphere at room temperature for 4 hours and 30 minutes. Acetone was added to the reaction mixture, and the mixture was concentrated under vacuum. 2 M hydrochloric acid and ethyl acetate were added to the residue for partition, and the aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with water, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under vacuum and the precipitate was washed with diethyl ether and n-hexane to obtain the title compound (529 mg, 87%). 1H-NMR Spectrum (DMSO-d6) delta (ppm): 4.61-4.74 (2H, m), 5.65-72 (1H, m), 6.97-7.7.03 (1H, m), 7.55-7.62 (1H, m), 12.92 (1H, brs).
Production Example 1165-{2- [5- (4-acetylpiperazin-l-yl) pyridin-2-yl] ethyl }thiophene- 2-carbohydrazide step 1 [0377] [0378]To a solution of 5-formylthiophene-2-carboxylic acid (2.000 g, 12.81 mmol) in tetrahydrofuran (25 ml) was added water (2.5 ml). Sodium borohydride (1.453 g, 38.42 mmol) was added by small portions, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was adjusted to pH about 8 by adding a small amount of IM hydrochloric acid, and washed with ethyl acetate. The aqueous layer was adjusted to pH 2 - 2.5 by adding concentrated hydrochloric acid, and saturated with sodium chloride. The mixture was extracted 3 times with ethyl acetate. The combined organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated to dryness to give 5-(hydroxymethyl) thiophene-2-carboxylic acid (1.430 g, yield 70.6%) as a yellow solid.
 

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