反応 #4091051
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-3b7a0fe531c44e8391a14c89759e0ea7表示可能な構造データがありません
N1(C)C(=O)CCCC1=O製品情報
1-methylpiperidine-2,6-dione (CAS 25077-25-2) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 161476
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
7 反応 · 7 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-3b7a0fe531c44e8391a14c89759e0ea7反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The Grignard reagent prepared in 300 ml of THF from 24 g (1.0 mole) of magnesium and 42 g (0.30 mole) of β-bromostyrene is decanted from excess metal and added dropwise under nitrogen to a solution of 27 g (0.21 moles) of N-methyl glutarimide at 3°- 5°. After 11/2 hrs. at room temperature, the mixture is treated with 250 ml of saturated NH4Cl solution with cooling. The separated aqueous layer is reextracted and the combined THF extracts washed with salt, dried over MgSO4 and freed of solvent. Product is extracted into hot ether and crystallized on cooling to yield white crystals, mp 108°- 112° C. is decanted from excess metal 2 hrs with cooling the combined THF extracts washed with salt dried over MgSO4 Product is extracted into hot ether crystallized on cooling to yield white crystals, mp 108°- 112° C.
ソース ID: ord-ecfd5e6d54e74309bff4d1113272e89d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The Grignard reagent prepared in 300 ml of THF from 24 g (1.0 mole) of magnesium and 42 g (0.30 mole) of β-bromostyrene is decanted from excess metal and added dropwise under nitrogen to a solution of 27 g (0.21 moles) of N-methyl glutarimide at 3°- 5°. After 11/2 hrs. at room temperature, the mixture is treated with 250 ml of saturated NH4Cl solution with cooling. The separated aqueous layer is reextracted and the combined THF extracts washed with salt, dried over MgSO4 and freed of solvent. Product is extracted into hot ether and crystallized on cooling to yield white crystals, mp 108°- 112° C. is decanted from excess metal 2 hrs with cooling the combined THF extracts washed with salt dried over MgSO4 Product is extracted into hot ether crystallized on cooling to yield white crystals, mp 108°- 112° C.
ソース ID: ord-ecfd5e6d54e74309bff4d1113272e89d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The Grignard reagent prepared in 300 ml of THF from 24 g (1.0 mole) of magnesium and 42 g (0.30 mole) of β-bromostyrene is decanted from excess metal and added dropwise under nitrogen to a solution of 27 g (0.21 moles) of N-methyl glutarimide at 3°- 5°. After 11/2 hrs. at room temperature, the mixture is treated with 250 ml of saturated NH4Cl solution with cooling. The separated aqueous layer is reextracted and the combined THF extracts washed with salt, dried over MgSO4 and freed of solvent. Product is extracted into hot ether and crystallized on cooling to yield white crystals, mp 108°- 112° C. is decanted from excess metal 2 hrs with cooling the combined THF extracts washed with salt dried over MgSO4 Product is extracted into hot ether crystallized on cooling to yield white crystals, mp 108°- 112° C.
ソース ID: ord-ecfd5e6d54e74309bff4d1113272e89d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-3b7a0fe531c44e8391a14c89759e0ea7反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The Grignard reagent prepared in 300 ml of THF from 24 g (1.0 mole) of magnesium and 42 g (0.30 mole) of β-bromostyrene is decanted from excess metal and added dropwise under nitrogen to a solution of 27 g (0.21 moles) of N-methyl glutarimide at 3°-5°. After 1 1/2 hrs. at room temperature, the mixture is treated with 250 ml of saturated NH4Cl solution with cooling. The separated aqueous layer is reextracted and the combined THF extracts washed with salt, dried over MgSO4 and freed of solvent. Product is extracted into hot ether and crystallized on cooling to yield white crystals, mp 108°-112°C. is decanted from excess metal After 1 1/2 hrs with cooling the combined THF extracts washed with salt dried over MgSO4 Product is extracted into hot ether crystallized on cooling to yield white crystals, mp 108°-112°C.
ソース ID: ord-51104cfd4e584a33ba824d08349edf7b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The Grignard reagent prepared in 300 ml of THF from 24 g (1.0 mole) of magnesium and 42 g (0.30 mole) of β-bromostyrene is decanted from excess metal and added dropwise under nitrogen to a solution of 27 g (0.21 moles) of N-methyl glutarimide at 3°- 5°. After 11/2 hrs. at room temperature, the mixture is treated with 250 ml of saturated NH4Cl solution with cooling. The separated aqueous layer is reextracted and the combined THF extracts washed with salt, dried over MgSO4 and freed of solvent. Product is extracted into hot ether and crystallized on cooling to yield white crystals, mp 108°- 112° C. is decanted from excess metal 2 hrs with cooling the combined THF extracts washed with salt dried over MgSO4 Product is extracted into hot ether crystallized on cooling to yield white crystals, mp 108°- 112° C.
ソース ID: ord-ecfd5e6d54e74309bff4d1113272e89dPubChem References
化合物の公開データベース記録に掲載された情報源です。
