関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | P-Cymene | HCID 7463 | — |
| 反応物 | Cyclohexane | HCID 8078 | — |
| 反応物 | 3,3-Dimethyl-1-butene | HCID 11210 | — |
| 反応物 | Aluminum(III) Chloride | HCID 6451240 | — |
| 生成物 | 1,1,3,4,4,6-Hexamethyltetralin | HCID 102750 | — |
反応手順
The starting material 1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene (HMT) was prepared by substantially following the procedures of Frank, U.S. Pat. No. 4,877,913. Specifically, a 100 ml, four-necked, round bottom flask was charged with cyclohexane (7.17 g) and anhydrous aluminum chloride (1.004 g), and cooled to about 16° C. A 60 ml addition funnel was charged with para-cymene (39.87 g), diisobutylene-2 (8.34 g), and neohexene (6.25 g) and connected to the flask. The funnel mixture was added to the flask over a period of about one hour and the flask mixture stirred 30 minutes following addition, while maintaining the temperature at about 16° C. The reaction was then quenched with deionized water (15 ml), and the organic phase separated and washed with, in order, 5% HCl, 10% Na2CO3, and 50% brine. The aqueous layers were then dried over K2CO3, filtered, and evaporated to yield a crude product (41.13 g) containing 28.16 weight % HMT.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05292719 |
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| 出典データセット | uspto-grants-1994_03 |
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| ORD ID | ord-72da079ef4fd4c10be586bd406d00419 |
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| 出典メモ | uspto-grants-1994_03 |
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