関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,2-Dichloroethane | HCID 11 | — |
| 反応物 | 1-Chloroethyl chloroformate | HCID 521305 | — |
| 反応物 | 1-(Diphenylmethyl)-3-[(2-methylprop-2-en-1-yl)oxy]azetidine | HCID 67154554 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-[(2-Methylprop-2-en-1-yl)oxy]azetidine hydrochloride | HCID 67154496 | — |
反応手順
A 16 mL flask was charged with 1-(diphenylmethyl)-3-[(2-methylprop-2-en-1-yl)oxy]azetidine (276 mg, 0.94 mmol; which may be prepared as described in Step 1) and 1,2-dichloroethane (4.1 mL). 1-Chloroethyl chloroformate (135 μL, 1.24 mmol) was added and the reaction mixture was stirred at 70° C. for 1.5 h. After cooling to room temperature, methanol (4.1 mL) was added and the reaction mixture was stirred at 70° C. for 1.5 h. The reaction mixture was concentrated to dryness and the residue was triturated in pentane to give the final product (192 mg, quantitative) as a brown oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846711B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-ac5eee5b523445c7b5b2ca05a5dd90c7 |
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| 出典メモ | uspto-grants-2014_09 |
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