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3-Phenoxybenzyl alcohol → 2,2-Dimethyl-3-(3-cyclopropylmethoxy-3-oxo-1-propenyl) cyclopropane-carboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Phenoxybenzyl alcohol | HCID 26295 | — |
| 反応物 | 2,2-Dimethyl-3-(3-cyclopropylmethoxy-3-oxo-1-propenyl) cyclopropane-carboxylic acid | HCID 53915596 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 2,2-Dimethyl-3-(3-cyclopropylmethoxy-3-oxo-1-propenyl) cyclopropane-carboxylic acid | HCID 53915596 | — |
| 生成物 | 2,2-Dimethyl-3-(3-cyclopropylmethoxy-3-oxo-1-propenyl)-cyclopropane-carboxylate | HCID 73675573 | — |
反応手順
Using the procedure of Example 9, m-phenoxy-benzyl alcohol and (1R, cis, ΔZ) 2,2-dimethyl-3-(3-cyclopropylmethoxy-3-oxo-1-propenyl)-cyclopropane-carboxylic acid were reacted to obtain m-phenoxy-benzyl (1R, cis, ΔZ) 2,2-dimethyl-3-(3-cyclopropylmethoxy-3-oxo-1-propenyl)-cyclopropane-carboxylate with a specific rotation of [α]D20 =+46.5°±2° (c=0.6% in chloroform).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04833163 |
| 出典データセット | uspto-grants-1989_05 |
| ORD ID | ord-f080ea205f164ce587c47687d5a85cb4 |
| 出典メモ | uspto-grants-1989_05 |