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Hydrochloric Acid → HCID 20528325、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Benzoin | HCID 8400 | — |
| 反応物 | Veratraldehyde | HCID 8419 | — |
| 反応物 | Potassium Cyanide | HCID 9032 | — |
| 反応物 | o-Fluorobenzaldehyde | HCID 67970 | — |
| 反応物 | 1,3-Diazepane-2-thione | HCID 736589 | — |
| 反応物 | 3,4-Dimethoxy-2'-fluorobenzoin | HCID 20528310 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | HCID 20528325 | HCID 20528325 | — |
反応手順
A mixture consisting of 16.6 g. of veratraldehyde, 12.5 g. of o-fluorobenzaldehyde, 8 g. of potassium cyanide, and 100 ml of 65% ethanol is reacted as described in Example 20, yielding 12.5 g. of 3,4-dimethoxy-2'-fluorobenzoin, m.p. 126°-128° C. A 5.8 g. portion of the benzoin derivative is converted to its methanesulfonate ester by the procedure of Example 20, giving 6.7 g. of the ester melting at 111°-113° C. 2.58 g. of the methanesulfonate ester, 0.91 g. of hexahydro-2H-1,3-diazepin-2-thione, and 55 ml. of acetone are mixed and left at room temperature for three days. 7 ml. of 2 N ethanolic hydrogen chloride are added, yielding 2.2 g. of the title compound, melting at 192°-194° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04344954 |
| 出典データセット | uspto-grants-1982_08 |
| ORD ID | ord-2c17cee5591046558cc1b46ca1a3b269 |
| 出典メモ | uspto-grants-1982_08 |