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HRID 1974181作成日:2026年10月27日

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

https://huagongshe.com/reaction/1974181

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 70577863—

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 was cooled to -78° and 2.5ml (18.8 mmole) of triethylamine was added followed by rapid addition of 35 ml (42mmole) of a 12% solution of phosgene in benzene. The mixture was stirred 15 min at -78°, 3 hours at -45°(acetonitrile-dry ice), then warmed to room temperature and concentrated to half volume in vacuo. To the resulting solution was added 50 ml of t-butanol and the mixture was stirred at room temperature overnight. The solvents were removed in vacuo and the residue diluted with ethyl acetate and filtered. The filtrate was transferred to a separatory funnel and washed with 5% aqueous sodium bicarbonate, 5% hydrochloric acid and brine, dried (MgSO4) and evaporated to dryness. Recrystallization of the crude, crystalline product from ether gave methyl cis-3-t-butoxycarbonylamino-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylate, mp 134°-135°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04000154
出典データセットuspto-grants-1976_12
ORD IDord-f1f7a722f9b94bf19da3bfbe3331e294
出典メモuspto-grants-1976_12