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Chemical Structure| 59967-06-5 Chemical Structure| 59967-06-5

Structure of 59967-06-5

Chemical Structure| 59967-06-5

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Product Details of [ 59967-06-5 ]

CAS No. :59967-06-5
Formula : C5H8O3S
M.W : 148.18
SMILES Code : CS(=O)(OC(C#C)C)=O
MDL No. :MFCD20039790

Safety of [ 59967-06-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 59967-06-5 ]

* 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 [ 59967-06-5 ]

[ 59967-06-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2914-69-4 ]
  • [ 124-63-0 ]
  • [ 59967-06-5 ]
YieldReaction ConditionsOperation in experiment
99% With triethylamine; In dichloromethane; at 0 - 20℃; for 2.5h; I(S(at)I-1-methylprop-2-ynyl methanesulfonate To a stirred solution of (S) -but-3-yn-2-ol (15g, 16.8ml, 0.2143mol), triethylamine (32.5g, 44.7ml, 0.3218mol) in dichloromethane (150ml) at 0C, was added dropwise over 30 minutes methanesulfonylchloride (29.4g, 19.9ml, 0.257mmol). The mixture was stirred for a further 2 hours before warming to ambient temperature. Water (150m.) was then added and the DCM layer was separated and the aqueous phase was extracted twice more (2 x 1 00ml). The combined organics were washed with brine (1 00ml) before drying over Na2S04. The solvent was removed under vacuo to yield a pale yellow oil/solid as the product (31.6g, 99%). GC-MS single peak Rt 1.4 minutes MS: 121, 120, 106, 77,68, 54,53, 51, 41 (No molecular ion)
95% With dmap; triethylamine; In dichloromethane; at 20℃; for 3h;Inert atmosphere; To a stirred solution of 15 (2.0 g, 28.5 mmol) in CH2Cl2 (50 mL) were added Et3N (6.0 mL, 42.8 mmol), MsCl (2.6 mL, 34.2 mmol) and DMAP (206 mg, 1.43 mmol) under the room temperature. After being stirred for 3 h, water (50 mL) was added at 0 C. The mixture was extracted with Et2O, washed with saturated NaHCO3 and brine, dried, concentrated and chromatographed (SiO2 58 g, hexane:Et2O = 3:2) to give 9 (4.0 g, 27.2 mmol, 95%) as a colorless oil. [alpha]D17-119.7 (c 1.11, CHCl3); 1H NMR (400 MHz, CDCl3) delta 5.29 (ddd, J = 2.0, 6.8, 13.2 Hz, 1H), 3.13 (s, 3H), 2.72 (d, J = 2.0 Hz, 1H), 1.66 (d, J = 6.8 Hz, 3H); 13C NMR (100 MHz, CDCl3) delta 80.1, 76.3, 67.4, 39.1, 22.4; FT-IR (KBr) 3283, 3029, 2998, 2942, 2125, 1358, 1177, 1123, 1090, 1017 cm-1; HRMS (EI) calcd for C5H7O3S [(M-H)+] 147.0116, found 147.0116.
 

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