참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methylparaben | HCID 7456 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2,2,2-Trifluoroethanesulfonyl chloride | HCID 74242 | — |
| 반응물 | 1-(Piperidin-1-yl)ethanol | HCID 3030541 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Amyl Acetate | HCID 12348 | — |
| 생성물 | 4-(2-Piperidinoethoxy)benzoic acid hydrochloride | HCID 5743835 | 93.2% |
반응 단계
Into a 50 ml round bottom flask is placed 4.93 g (27.0 mmol) of 2,2,2-trifluoroethanesulfonyl chloride and 25 ml of methylene chloride. The resulting solution is cooled with an ice bath as 3.22 g (24.9 mmol) of 1-piperidinoethanol in 7 ml of methylene chloride is added dropwise. After the addition is complete, the ice bath is removed and the resulting slurry is stirred for about 12 hours. The reaction mixture is concentrated on a rotary evaporator to yield a waxy residue. The solid residue is slurried in 45 ml of amyl acetate and then potassium carbonate (5.50 g, 39.9 mmol) and methyl 4-hydroxybenzoate (2.26 g, 14.8 mmol) are added. The resulting mixture is heated to 140° C. for 2 hours. The reaction mixture is cooled to room temperature and washed twice with water and the organic layer is extracted with 10.5 ml of 8 N hydrochloric acid. The aqueous layer is heated at gentle reflux for 4 hours. The resulting slurry is cooled to 50° C. and 11 ml of acetone is added. The slurry is cooled to 0-5° C. and stirred for 1 hour. The product is filtered, washed with cold acetone, and dried at 50° C. in vacuo to yield 3.94 g of product, (90%). 1H NMR. HPLC 96.9%. TRS 2.78%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06075146 |
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| 출처 데이터셋 | uspto-grants-2000_06 |
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| ORD ID | ord-a468fc0052b347668176a6bfc4de27e6 |
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| 출처 메모 | uspto-grants-2000_06 |
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