참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Stearyl Alcohol | HCID 8221 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 반응물 | 2-(4-tert-Butyl-3-hydroxy-2,6-dimethylphenyl)acetic acid | HCID 20345905 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | n-Octadecyl 4-tert.-butyl-2,6-dimethyl-3-hydroxyphenylacetate | HCID 20345920 | — |
반응 단계
10.68 grams of the compound of Example 5, 11.4 grams of n-octadecanol and 0.8 grams of p-toluene sulfonic acid monohydrate were dispersed in 150 ml of toluene and heated at reflux for seven hours during which the water collected by azeotropic distillation was almost equal to the theory. The reaction mixture was successively washed with water, aqueous saturated sodium bicarbonate solution, and then with water once again until the wash water was neutral. After drying over anhydrous sodium sulfate and filtering free of the drying agent, the clear filtrate was evaporated at reduced pressures to yield the desired product as residue. After successive crystallizations from acetonitrile and n-heptane, the desired compound was isolated as white crystals melting at 57° to 59° C. (Compound 1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04196301 |
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| 출처 데이터셋 | uspto-grants-1980_04 |
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| ORD ID | ord-57ca0523165445c687ffdbc6dda8ee86 |
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| 출처 메모 | uspto-grants-1980_04 |
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