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4-Cyanophenol → 2,2-dimethyl-2H-1-benzopyran-6-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Cyanophenol | HCID 13019 | — |
| 反応物 | 1-Butyne, 3-chloro-3-methyl- | HCID 70679 | — |
| 溶媒 | Propargyl ether | HCID 23349 | — |
| 生成物 | 2,2-dimethyl-2H-1-benzopyran-6-carbonitrile | HCID 2779074 | — |
反応手順
According to EPO 0 076 075 describing the possibilities for preparing Kromakalim 4-cyano-phenol of the formula (I) ##STR4## is reacted with 3-chloro-3-methyl-butyne resulting in propargyl-ether of the formula (IX) ##STR5## which is then subjected to ring closure to produce 6-cyano-2,2-dimethyl-2H-1-benzopyran of the formula (III) ##STR6## The compound of the formula (III) is then converted through 6-cyano-trans-3-bromo-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-ol to 6-cyano-3,4-dihydro-3,4-epoxy-2,2-dimethyl-2H-1-benzopyran of the formula (V). ##STR7## From the compound of the formula (V) the end-product of the formula (VI) can be obtained by three independent routes.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05145985 |
| 出典データセット | uspto-grants-1992_09 |
| ORD ID | ord-88f13fcc82b9429998671f5d129e5036 |
| 出典メモ | uspto-grants-1992_09 |