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Chemical Structure| 873330-01-9 Chemical Structure| 873330-01-9

Structure of 873330-01-9

Chemical Structure| 873330-01-9

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Product Details of [ 873330-01-9 ]

CAS No. :873330-01-9
Formula : C14H21NO2S
M.W : 267.39
SMILES Code : O=C(NCCSCC1=CC=CC=C1)OC(C)(C)C
MDL No. :MFCD09839993

Safety of [ 873330-01-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 873330-01-9 ]

* 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 [ 873330-01-9 ]

[ 873330-01-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 100-53-8 ]
  • [ 158690-56-3 ]
  • [ 873330-01-9 ]
YieldReaction ConditionsOperation in experiment
83% With caesium carbonate; In N,N-dimethyl-formamide; for 18h; 67C: N-Boc-2-Benzylsulfanyl-ethylamine; N-Boc-2-Tosyl-ethylamine (100 mg, 0.32 mmol) was added to a mixture of benzylmercaptan (45 mL, 0.38 mmol) and CsaCOs (68 mg, 0.21 mmol) in 1.6 mL of dry DMF. The reaction was stirred for 18 hours after which time the reaction mixture was poured onto water. The aqueous layer was extracted three times with AcOEt. The combined organic layers were washed with water, saturated NaHCOs and brine, dried over Na2SC>4 and concentrated. The residue was purified using SiC>2 with AcOEt/Petroleum ether 5:95 to 15:75. A yellow oil was obtained (72 mg, 83%). NMR 'H (ppm, CDC13): 7.31-7.25 (m, 5H), 4.79 (br. s., 1H), 3.70 (s, 2H), 3.25 (m, 2H), 2.55-2.53 (m, 2H), 1.43 (s, 9H).
83% With caesium carbonate; In N,N-dimethyl-formamide; for 18h; 67C: N-Boc-2-Benzylsulfanyl-ethylamine; N-Boc-2-Tosyl-ethylamine (100 mg, 0.32 mmol) was added to a mixture of benzylmercaptan (45 mL, 0.38 mmol) and Cs2CO3 (68 mg, 0.21 mmol) in 1.6 mL of dry DMF. The reaction was stirred for 18 hours after which time the reaction mixture was poured onto water. The aqueous layer was extracted three times with AcOEt. The combined organic layers were washed with water, saturated NaHCO3 and brine, dried over Na2SO4 and concentrated. The residue was purified using SiO2 with AcOEt/Petroleum ether 5:95 to 15:75. A yellow oil was obtained (72 mg, 83%). NMR 1H (ppm, CDCl3): 7.31-7.25 (m, 5H), 4.79 (br. s., 1H), 3.70 (s, 2H), 3.25 (m, 2H), 2.55-2.53 (m, 2H), 1.43 (s, 9H).
 

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