反応 #4152666
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-841e8dfc43e242bea3a5aa416925b428表示可能な構造データがありません
CCCCCC(C(=O)OCC)Br製品情報
ethyl 2-bromoheptanoate (CAS 5333-88-0) 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 95333
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-841e8dfc43e242bea3a5aa416925b428反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-305836022b8e44ab8e8952b704534f93反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-841e8dfc43e242bea3a5aa416925b428反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: When in the general procedure of Example 71 an appropriate amount of 5-dodecyl-1H-tetrazole was substituted for 5-decyl-1H-tetrazole and an appropriate amount of ethyl-2-bromoheptanoate was substituted for ethyl 2-bromophenylacetate, the title compound was obtained.
ソース ID: ord-b328ce5afa974e3db995419ca61bd939反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: When in the general procedure of Example 71 an appropriate amount of 5-dodecyl-1H-tetrazole was substituted for 5-decyl-1H-tetrazole and an appropriate amount of ethyl-2-bromoheptanoate was substituted for ethyl 2-bromophenylacetate, the title compound was obtained.
ソース ID: ord-b328ce5afa974e3db995419ca61bd939反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(4-Methoxy-phenylsulfanyl)-heptanoic acid ethyl ester (13.8 g, 98%) was prepared according to the general method as outlined in example 1 starting from ethyl 2-bromoheptanoate (11 g, 47 mmol) and 4-methoxythiophenol (6 g, 42.8 mmol), as a yellow oil; MS: 297.2 (M+H)+.
ソース ID: ord-a24c4c085352445a978f1232c59e598c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(4-Methoxy-phenylsulfanyl)-heptanoic acid ethyl ester (13.8 g, 98%) was prepared according to the general method as outlined in example 1 starting from ethyl 2-bromoheptanoate (11 g, 47 mmol) and 4-methoxythiophenol (6 g, 42.8 mmol), as a yellow oil; MS: 297.2 (M+H)+.
ソース ID: ord-a24c4c085352445a978f1232c59e598c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(4-Methoxy-phenylsulfanyl)-heptanoic acid ethyl ester (13.8 g, 98%) was prepared according to the general method as outlined in example 1 starting from ethyl 2-bromoheptanoate (11 g, 47 mmol) and 4-methoxythiophenol (6 g, 42.8 mmol), as a yellow oil; MS: 297.2 (M+H)+.
ソース ID: ord-a53a1964600640f78d7b0b70da2f559b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: When in the general procedure of Example 71 an appropriate amount of 5-dodecyl-1H-tetrazole was substituted for 5-decyl-1H-tetrazole and an appropriate amount of ethyl-2-bromoheptanoate was substituted for ethyl 2-bromophenylacetate, the title compound was obtained.
ソース ID: ord-b328ce5afa974e3db995419ca61bd939反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-305836022b8e44ab8e8952b704534f93反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: When in the general procedure of Example 71 an appropriate amount of 5-dodecyl-1H-tetrazole was substituted for 5-decyl-1H-tetrazole and an appropriate amount of ethyl-2-bromoheptanoate was substituted for ethyl 2-bromophenylacetate, the title compound was obtained.
ソース ID: ord-16d5ef9fa43740c6ae5e6ad635e06210反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: When in the general procedure of Example 71 an appropriate amount of 5-dodecyl-1H-tetrazole was substituted for 5-decyl-1H-tetrazole and an appropriate amount of ethyl-2-bromoheptanoate was substituted for ethyl 2-bromophenylacetate, the title compound was obtained.
ソース ID: ord-16d5ef9fa43740c6ae5e6ad635e06210PubChem 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。
