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[ CAS No. 50675-23-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 50675-23-5
Chemical Structure| 50675-23-5
Structure of 50675-23-5 * Storage: {[proInfo.prStorage]}
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Product Details of [ 50675-23-5 ]

CAS No. :50675-23-5 MDL No. :MFCD11054023
Formula : C8H16O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 144.21 Pubchem ID :-
Synonyms :

Safety of [ 50675-23-5 ]

Signal Word:Warning Class:
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313 UN#:
Hazard Statements:H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 50675-23-5 ]

* 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 [ 50675-23-5 ]

[ 50675-23-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 50675-23-5 ]
  • [ 50675-25-7 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: dmap; pyridine / dichloromethane / 18 h / 20 °C 2: ammonia / tetrahydrofuran / -78 - 125 °C
Multi-step reaction with 2 steps 1: dmap; pyridine / dichloromethane / 18 h / 20 °C 2: ammonia / tetrahydrofuran / 18 h / -78 - 125 °C
Multi-step reaction with 2 steps 1: dmap; pyridine / dichloromethane / 18 h / 20 °C 2: ammonia / tetrahydrofuran / 18 h / -78 - 125 °C / Autoclave
Multi-step reaction with 2 steps 1: dmap; triethylamine / dichloromethane / 18 h / 20 °C 2: ammonia / tetrahydrofuran / 18 h / 125 °C
Multi-step reaction with 2 steps 1: pyridine / dmap / dichloromethane / 18 h / 20 °C 2: ammonia / tetrahydrofuran / 18 h / -78 - 125 °C
Multi-step reaction with 2 steps 1: dmap; pyridine / dichloromethane / 18 h / 20 °C 2: ammonia / tetrahydrofuran / 18 h / 125 °C
Multi-step reaction with 2 steps 1: pyridine; dmap / dichloromethane / 18 h / 20 °C 2: ammonia / tetrahydrofuran / 18 h / -78 - 125 °C
Multi-step reaction with 2 steps 1: pyridine; dmap / dichloromethane / 18 h / 20 °C 2: ammonia / tetrahydrofuran / 18 h / 125 °C / steel bomb

  • 2
  • [ 52916-16-2 ]
  • [ 50675-23-5 ]
YieldReaction ConditionsOperation in experiment
With borane-THF; In tetrahydrofuran; at 0℃; for 2h; Intermediate 071 (2,2-Dimethyltetrahydro-2H-pyran-4-yl)methanol <strong>[52916-16-2]2,2-Dimethyltetrahydro-2H-pyran-4-carboxylic acid</strong> (820 mg, 5.18 mmol) was dissolved in tetrahydrofuran (16 mL). At 0 C BH3-tetrahydrofuran-complex (668 mg, 7.78 mmol) was added and stirred for another 2 hours at 0 C. It was quenched with saturated ammonium chloride solution, the organic solvent was removed in vacuo, water was added and it was extracted twice with ethyl acetate. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. As GC-MS showed only 50% conversion the same procedure was repeated leading to crude (2,2-dimethyltetrahydro-2H-pyran-4-yl)methanol (491 mg) which was used in the next step without further purification.
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