Simple exploration of 171877-39-7

As the paragraph descriping shows that 171877-39-7 is playing an increasingly important role.

171877-39-7, (S)-4-Benzylthiazolidine-2-thione is a thiazolidine compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

The product was synthesizedfollowing a previously reported procedure.1 To a solution of (S)-4-benzylthiazolidine-2-thione(0.15 g, 0.72 mmol) and triethylamine (0.11 mL, 0.79 mmol) in DCM (1.1 mL) at 0 C wasadded dropwise a solution of butyryl chloride (0.078 mL, 0.75 mmol) dissolved in DCM (0.3mL) over 2 min. The vial containing the butyryl chloride solution was rinsed with additionalDCM (0.3 mL) which was added to the reaction. The reaction was warmed to room temperatureand stirred for 4.5 h. The reaction was then quenched with water and the organic layer wasseparated from the aqueous phase. The aqueous phase was extracted three times with DCM.The combined organic layers was washed with brine and dried with anhydrous Na2SO4. Thesuspension was filter and volatile materials were removed using a rotary evaporator. The crudematerial was purified via silica gel flash chromatography (7% acetone in hexanes) to yield 0.169g of product as a yellow solid (84% yield). The resonances in the 1H NMR and 13C spectrum ofthe product matched previously reported chemical shifts.1

As the paragraph descriping shows that 171877-39-7 is playing an increasingly important role.

Reference£º
Article; Huang, David S.; Wong, Henry L.; Georg, Gunda I.; Bioorganic and Medicinal Chemistry Letters; vol. 28; 16; (2018); p. 2789 – 2793;,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com

Brief introduction of 171877-39-7

171877-39-7 (S)-4-Benzylthiazolidine-2-thione 11458470, athiazolidine compound, is more and more widely used in various.

171877-39-7, (S)-4-Benzylthiazolidine-2-thione is a thiazolidine compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: Thiazolidine-2-thione 2 (2.5 mmol), benzyl chloride (317 mg, 2.5 mmol), and K2CO3(691 mg, 5 mmol) were dissolved in 10 mL of acetone. The resulting solution was refluxedfor 2-4 h under TLC monitoring and then was allowed to cool to r.t. and filtered. Afterremoval of the solvent, the crude product was obtained and purified by silica-gel columnchromatography with a mixture of petroleum ether and EtOAc (10:1, v/v) as eluent.

171877-39-7 (S)-4-Benzylthiazolidine-2-thione 11458470, athiazolidine compound, is more and more widely used in various.

Reference£º
Article; Chen, Ning; Du, Hongguang; Liu, Weidong; Wang, Shanshan; Li, Xinyao; Xu, Jiaxi; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 190; 1; (2015); p. 112 – 122;,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com