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HRID 616154作成日:2026年10月25日

Toluene → Methyl cis-3-t-butoxycarbonylamino-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylate

https://huagongshe.com/reaction/616154

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物PhosgeneHCID 6371—
反応物TriethylamineHCID 8471—
反応物Methyl cis-1-(2,4-Dimethoxybenzyl)-3-amino-4-oxoazetidine-2-carboxylateHCID 18632686—
反応物Acetonitrile dry iceHCID 86587134—
溶媒BenzeneHCID 241—
生成物Methyl cis-3-t-butoxycarbonylamino-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylateHCID 7057786352%

反応手順

A solution of 5.5 g (18.8 mmole) of methyl cis-3-amino-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylate in 100 ml of dry toluene is cooled to -78°; 2.5 ml (18.8 mmole) of triethylamine is added followed by rapid addition of 35 ml (42 mmole) of a 12% solution of phosgene in benzene. The mixture is stirred 15 min at -78°, 3 hr at -45° (acetonitrile-dry ice), then warmed to room temperature and concentrated to half volume in vacuu. To the resulting solution is added 50 ml of t-butanol and the mixture is stirred at room temperature overnight. The solvents are removed in vacuum, the residue is diluted with ethyl acetate and filtered. The filtrate is transferred to a separatory funnel and washed with 5% Na HCO3, 5% HCl and brine; dried over magnesium sulfate and evaporated to dryness. Recrystallization of the crude, crystalline product affords 3.8 g (52%) of the title compound. Recrystallization from ether gives an analytical sample.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04072674
出典データセットuspto-grants-1978_02
ORD IDord-2587c0ec3bd24ec29bd4f74911afc430
出典メモuspto-grants-1978_02