反応 #4041065
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-2e7293a163e04c11a9091bdfc663b829表示可能な構造データがありません
CCCCCCCCCCCCCC=CC製品情報
hexadec-2-ene (CAS 26741-29-7) 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 525020
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-2e7293a163e04c11a9091bdfc663b829反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A process according to claim 1, wherein (a) is 1-decene or 9-octadecene and (b) is a mixture of 2-tetradecene with 2-hexadecene or 1-pentadecene, whereby a mixture of 9-tricosene and 9-heneicosene is formed.
ソース ID: ord-bddd77911add47dcaa1ee803c4328848反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 9-triscosene and 9-heneicosene was prepared by following the process described in Example 8, namely by conducting, over 39 g. of the aforedescribed rehenium-containing catalyst, at 60° C., a mixture of 196 g. (0.79 mole) of 9-octadecene, 58 g. (0.26 mole) of 2-hexadecene, and 16 g. (0.08 mole) of 2-tetradecene. After a reaction time of 5 hours and with a throughput of 200 ml. of olefin mixture per hour, 3.2% by weight of tricosene and 1.4% by weight of heneicosene were obtained. The content of the cis-isomer was 24%. was prepared of the aforedescribed rehenium-containing catalyst, at 60° C., a mixture of 196 g After a reaction time of 5 hours
ソース ID: ord-cb5d6c1b684c40629bccade648677b7a反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Following the procedure outlined in Example 6, 142 g. (0.56 mole) of 9-octadecene and 82 g. (0.37 mole) of 2-hexadecene were reacted at a reaction temperature of 100° C. After 5 hours and with a throughput of 200 ml. of olefin mixture per hour, 7.4% by weight of tricosene was obtained.
ソース ID: ord-9b85832f49d94ce5a2302cb1e440356e反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A process according to claim 1, wherein (a) is 1-decene or 9-octadecene and (b) is a mixture of 2-tetradecene with 2-hexadecene or 1-pentadecene, whereby a mixture of 9-tricosene and 9-heneicosene is formed.
ソース ID: ord-bddd77911add47dcaa1ee803c4328848反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 9-triscosene and 9-heneicosene was prepared by following the process described in Example 8, namely by conducting, over 39 g. of the aforedescribed rehenium-containing catalyst, at 60° C., a mixture of 196 g. (0.79 mole) of 9-octadecene, 58 g. (0.26 mole) of 2-hexadecene, and 16 g. (0.08 mole) of 2-tetradecene. After a reaction time of 5 hours and with a throughput of 200 ml. of olefin mixture per hour, 3.2% by weight of tricosene and 1.4% by weight of heneicosene were obtained. The content of the cis-isomer was 24%. was prepared of the aforedescribed rehenium-containing catalyst, at 60° C., a mixture of 196 g After a reaction time of 5 hours
ソース ID: ord-cb5d6c1b684c40629bccade648677b7a反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 9-triscosene and 9-heneicosene was prepared by following the process described in Example 8, namely by conducting, over 39 g. of the aforedescribed rehenium-containing catalyst, at 60° C., a mixture of 196 g. (0.79 mole) of 9-octadecene, 58 g. (0.26 mole) of 2-hexadecene, and 16 g. (0.08 mole) of 2-tetradecene. After a reaction time of 5 hours and with a throughput of 200 ml. of olefin mixture per hour, 3.2% by weight of tricosene and 1.4% by weight of heneicosene were obtained. The content of the cis-isomer was 24%. was prepared of the aforedescribed rehenium-containing catalyst, at 60° C., a mixture of 196 g After a reaction time of 5 hours
ソース ID: ord-cb5d6c1b684c40629bccade648677b7a反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Following the procedure outlined in Example 6, 142 g. (0.56 mole) of 9-octadecene and 82 g. (0.37 mole) of 2-hexadecene were reacted at a reaction temperature of 100° C. After 5 hours and with a throughput of 200 ml. of olefin mixture per hour, 7.4% by weight of tricosene was obtained.
ソース ID: ord-9b85832f49d94ce5a2302cb1e440356e反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2e7293a163e04c11a9091bdfc663b829反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A process according to claim 1, wherein (a) is 1-decene or 9-octadecene and (b) is a mixture of 2-tetradecene with 2-hexadecene or 1-pentadecene, whereby a mixture of 9-tricosene and 9-heneicosene is formed.
ソース ID: ord-bddd77911add47dcaa1ee803c4328848反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 9-triscosene and 9-heneicosene was prepared by following the process described in Example 8, namely by conducting, over 39 g. of the aforedescribed rehenium-containing catalyst, at 60° C., a mixture of 196 g. (0.79 mole) of 9-octadecene, 58 g. (0.26 mole) of 2-hexadecene, and 16 g. (0.08 mole) of 2-tetradecene. After a reaction time of 5 hours and with a throughput of 200 ml. of olefin mixture per hour, 3.2% by weight of tricosene and 1.4% by weight of heneicosene were obtained. The content of the cis-isomer was 24%. was prepared of the aforedescribed rehenium-containing catalyst, at 60° C., a mixture of 196 g After a reaction time of 5 hours
ソース ID: ord-cb5d6c1b684c40629bccade648677b7a反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Following the procedure outlined in Example 6, 142 g. (0.56 mole) of 9-octadecene and 82 g. (0.37 mole) of 2-hexadecene were reacted at a reaction temperature of 100° C. After 5 hours and with a throughput of 200 ml. of olefin mixture per hour, 7.4% by weight of tricosene was obtained.
ソース ID: ord-9b85832f49d94ce5a2302cb1e440356ePubChem 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。
