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Bromobenzene → tert-butyl N-[2-(1-phenylpiperidin-4-yl)ethyl]carbamate

HRID 223
ノート
印刷プレビュー

反応式

HRID 223 の反応式
Brc1ccccc1.CC(C)(C)OC(=O)NCCC1CCNCC1>CC(=O)O.CC(=O)O.CC(C)(C)[O-].CC1(C)c2cccc(P(c3ccccc3)c3ccccc3)c2Oc2c(P(c3ccccc3)c3ccccc3)cccc21.Cc1ccccc1.[Na+].[Pd]>CC(C)(C)OC(=O)NCCC1CCN(c2ccccc2)CC1
参加物反応条件実験手順出典と根拠反応ノート

参加物

7

反応物 2

HCID 7961BromobenzeneHCID 15018494-(2-Aminoethyl)piperidine, 4-BOC protected

生成物 1

HCID 69152784tert-butyl N-[2-(1-phenylpiperidin-4-yl)ethyl]carbamate収率 0%

試薬・触媒・溶媒 4

HCID 23676156Sodium t-butoxide試薬HCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)触媒

反応条件

温度
50 °C

実験手順

palladium(II) acetate (21.45 mg, 0.10 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (111 mg, 0.19 mmol) were placed in a round-bottomed vessel that was filled with nitrogen. Toluene (0.8 mL) was added and the mixture was heated to 50°C for 30 min. sodium tert-butoxide (138 mg, 1.43 mmol) was added to a second vessel and inerted with nitrogen. tert-butyl 2-(piperidin-4-yl)ethylcarbamate (342 mg, 1.5 mmol) and bromobenzene (150mg, 0.96 mmol) and toluene (1.4 mL) were added. 14/04 2009 13:57:24 +0200 The catalyst solution was added to the reagent mixture and the combined mixture was heated to reflux for several hours. The reaction did not work.

出典と根拠

ORDレコード
ord-59ade4a657944ddaa87cf04392b14d28
出典データセット
750 AstraZeneca ELN dataset
元リンク
出典を表示

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順出典と根拠反応ノート
HCID 4144353
Palladium (II) acetate
触媒
HCID 1140Toluene溶媒