反応 #4139729
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-8f2a25738cd649ec9ed31fc05ef5c0aa表示可能な構造データがありません
C1COC1製品情報
oxetane (CAS 503-30-0) 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 10423
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
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8f2a25738cd649ec9ed31fc05ef5c0aa反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-27779a1629e54e38bcc93e0438966156反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ebe2c5cdced546c794841a5efecd155f反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-80f053ba3d1d4e26b518accb2353d27c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-dc24f0b3e41e44b29fa1669f395d38df反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: N-Butyllithium in hexane (1.5M; 35.6 ml) was added dropwise at room temperature under nitrogen to a solution of 2-methylthiophene (5.0 g) in dry THF (50 ml). After stirring for 2.25 h, oxetane (4.42 g) in dry THF (15 ml) was added dropwise and stirring continued for 22.5 h. Saturated ammonium chloride solution (200 ml) was added and the mixture extracted with diethyl ether (3×200 ml), dried and evaporated in vacuo to give an oil. Purification by FCC on silica gel with cyclohexane-diethyl ether (1:1) as eluent gave the title compound as a pale orange oil (1.4 g). T.l.c. (cyclohexane-diethyl ether 1:1) Rf 0.31. stirring continued for 22.5 h the mixture extracted with diethyl ether (3×200 ml) dried evaporated in vacuo to give an oil Purification by FCC on silica gel with cyclohexane-diethyl ether (1:1) as eluent
ソース ID: ord-94e69922e1744a8b9c6ce56a4c41268f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: According to the ratio for charging as described in Table 2, oxetane and delta-valerolactone (referred to as VL in Table and Figure) were mixed, and polymerized in a bulk state at 60° C. for 24 hours using 0.2% by mol of a triethylaluminum-water (1/0.75) based complex as an initiator based on the total amount of the monomers. were mixed polymerized in a bulk state at 60° C. for 24 hours
ソース ID: ord-5eb6cc29799f4320bb7fc3e47e0a4563反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 22.7 grams (0.1 mole) of 3-(4-propylheptyl)morpholine, 6.4 grams (0.11 moles) trimethyleneoxide and 150 ml. 96% ethanol was kept at 150°-200° C. for 15 hours in an autoclave. Distillation of the reaction mixture gave 24.6 g (86%) of 3-(4-propyl-heptyl)-4-(3-hydroxypropyl)morpholine), boiling point 122°-124° C./0.01 mm Hg. Distillation of the reaction mixture
ソース ID: ord-b8208c849c4f46cd9f4ac68eac7a570b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 20 g. of oxetane (0.34 mole), 32.8 g. of N,N,N-trimethyl-[3-(methylamino)]-1-propanaminium bromide (0.156 mole) and 22 ml. water is heated in a sealed tube at 100° for 15 hours. The solution is evaporated in vacuo and the residue is dissolved in 50 ml. of acetonitrile and filtered. Upon evaporation the desired product crystallizes. The product may be recrystallized from acetonitrile. A mixture of 20 g The solution is evaporated in vacuo the residue is dissolved in 50 ml of acetonitrile and filtered Upon evaporation the desired product crystallizes The product may be recrystallized from acetonitrile
ソース ID: ord-44653225d6c84dd7a50b91061a254dd2反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8f2a25738cd649ec9ed31fc05ef5c0aa反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8f2a25738cd649ec9ed31fc05ef5c0aa反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-27779a1629e54e38bcc93e0438966156PubChem 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。
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