反応 #4136174
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-23a04c29288740ca9e134c48c99ecf53表示可能な構造データがありません
COC(=O)CCCCCCCBr製品情報
methyl 8-bromooctanoate (CAS 26825-92-3) 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 11107373
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-23a04c29288740ca9e134c48c99ecf53反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b29babbed6424607a076f33edff3588b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9e572b3acde1482cb8b61730f75edb4d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6b3c481f8bbf482ab746ed342fe16402反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6b353c95bfe8400c9bc8da5e31e59aab反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-e67b8344a20349fd816e1fac34519307反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The product is produced as described in example 1 from 0.75 g. of NaH (80% suspension in mineral oil), 5.6 g. of 1-benzylbenzimidazolin-2-one (produced in usual manners by alkylation of benzimidazolin-2-one with benzylchloride according to example 8), 50 cc. of DMF, 5.9 g. of 8-bromocaprylic acid methyl ester and 0.75 g. of NaJ. The product is produced
ソース ID: ord-fdb769078caf46fbb94c01b9cc831d09反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The product is produces as described in example 1 from 1.2 g. of NaH (80% suspension in mineral oil), 9.8 g. of 1-(3-chlorophenyl)-benzimidazolin-2-one, 80 cc. of DMF, 9.5 g. of 8-bromocaprylic acid methyl ester and 1.2 g. of NaJ. The product is produces
ソース ID: ord-7468b507969d40f5a1f52fd93840d01c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The product is produced as described in example 1 from 0.9 g. of NaH (80% suspension in mineral oil), 7.5 g. of 1-octylbenzimidazolin-2-one (produced) by alkylation from benzimidazolin-2-one with bromooctane according to example 8), 100 cc. of DMF, 7.1 g. of 8-bromocaprylic acid methyl ester and 0.9 g. of NaJ. Eluant in chromatographic purification: hexane/ethylacetate. The product is produced Eluant in chromatographic purification
ソース ID: ord-cb6ba25dbe284f008800d616d4b95ef7反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The product is produced as described in example 1 from 2.8 g. of NaH (80% suspension in mineral oil), 25 g. of benzimidazolin-2-one, 180 cc. of DMF, 22.1 g. of 8-bromocaprylic acid methyl ester and 2.8 g. of NaJ. Eluant in chromatographic purification: chloroform/methanol. The product is produced Eluant in chromatographic purification
ソース ID: ord-fefd9dabde024563a0c8f52b4a7146f2反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The product is produced as described in example 1 from 3 g. of NaH (80% suspension in mineral oil), 15.1 g. of benzthiazolin-2-one, 200 cc. of DMF, 23.7 g. of 8-bromo-caprylic acid methyl ester and 3 g. NaJ. The product is produced
ソース ID: ord-addf4e48275b4874a28b8f3d64b11e27反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The product is produced as described in example 1 from 3 g. of NaH (80% suspension in mineral oil), 17 g. of 5-chloro-benzoxazolin-2-one (produced in usual manners by subjecting 2-amino-4-chloro-phenol-hydrochloride to reaction with phosgene), 200 cc. of DMF, 23.7 g. of 8-bromo-caprylic acid methyl ester and 3 g. of NaJ. The product is produced
ソース ID: ord-1276cb9699e947f78b4dcbe8f2f4cf38PubChem 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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