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HRID 234490作成日:2026年10月26日

Benzyl Bromide → Benzyl 6-(tert-butoxycarbonylamino)hexanoate

https://huagongshe.com/reaction/234490

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物6-((tert-Butoxycarbonyl)amino)hexanoic acidHCID 637602—
溶媒DichloromethaneHCID 6344—
生成物Benzyl 6-(tert-butoxycarbonylamino)hexanoateHCID 12160267—

反応手順

1.94 ml of DBU and then 1.54 ml of benzyl bromide are added at RT to a solution of 3 g of 6-(tert-butoxycarbonylamino)hexanoic acid in 60 ml of DCM and the mixture is stirred for 24 hours at RT. It is concentrated under vacuum, the residue is taken up with 100 ml of water and extracted with AcOEt, the organic phase is washed with a 5% solution of potassium carbonate, with a saturated solution of NaCl and with water and dried over sodium sulfate and the solvent is evaporated off under vacuum to give 2.8 g of the expected product, which is used as such.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05594023
出典データセットuspto-grants-1997_01
ORD IDord-f9b768c700394298bbbed1554bf678e4
出典メモuspto-grants-1997_01