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Chemical Structure| 912669-58-0 Chemical Structure| 912669-58-0

Structure of 912669-58-0

Chemical Structure| 912669-58-0

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Product Details of [ 912669-58-0 ]

CAS No. :912669-58-0
Formula : C3H3ClN2OS
M.W : 150.59
SMILES Code : OCC1=NN=C(Cl)S1
MDL No. :MFCD14155682

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Application In Synthesis of [ 912669-58-0 ]

* 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 [ 912669-58-0 ]

[ 912669-58-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 64837-49-6 ]
  • [ 912669-58-0 ]
YieldReaction ConditionsOperation in experiment
75% With sodium borohydrid; In methanol; Preparation 39 Synthesis of (5-chloro-1,3,4-thiadiazol-2-yl)methanol To a solution of <strong>[64837-49-6]ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate</strong> (0.51 g, 2.60 mmol) in anhydrous methanol (5.00 mL) was added sodium borohydride (0.30 g, 7.99 mmol) at 0 C. The reaction mixture was stirred at ambient temperature for 16 h, diluted with acetic acid (3.00 mL) and extracted with ethyl acetate (2*150 mL). The combined organics was washed with aqueous saturated sodium bicarbonate (3*25.0 mL) and aqueous saturated sodium chloride (2*25.0 mL). The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to dryness to give the title compound (0.30 g, 75%) as a light yellow semi-solid: 1H NMR (300 MHz, CDCl3) delta 5.04 (s, 2H), 2.80 (br, 1H); MS (ES+) 151.1 (M+1), 153.1 (M+1).
75% With sodium tetrahydroborate; In methanol; at 0 - 20℃; for 16.0h; To a a solution of <strong>[64837-49-6]ethyl 5-chloro-1 ,3,4-thiadiazole-2-carboxylate</strong> (0.51 g, 2.60 mmol) in anhydrous methanol (5.00 mL) was added sodium borohydride (0.30 g, 7.99 mmol) at 0 0C. The reaction mixture was stirred at ambient temperature for 16 h, diluted with acetic acid (3.00 mL) and extracted with ethyl acetate (2 x 150 mL). The combined organics was washed with aqueous saturated sodium bicarbonate (3 x 25.0 mL) and aqueous saturated sodium chloride (2 x 25.0 mL). The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to dryness to give the title compound (0.30 g, 75%) as a light yellow semi-solid: 1H NMR (300 MHz, CDCI3) delta 5.04 (s, 2H), 2.80 (br, 1 H); MS (ES+) 151.1 (M + 1), 153.1 (M + 1).
 

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