関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Phosgene | HCID 6371 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methyl cis-1-(2,4-Dimethoxybenzyl)-3-amino-4-oxoazetidine-2-carboxylate | HCID 18632686 | — |
| 反応物 | Acetonitrile dry ice | HCID 86587134 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | Methyl cis-3-t-butoxycarbonylamino-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04000154 |
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| 出典データセット | uspto-grants-1976_12 |
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| ORD ID | ord-f1f7a722f9b94bf19da3bfbe3331e294 |
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| 出典メモ | uspto-grants-1976_12 |
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