참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methylparaben | HCID 7456 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Amyl Acetate | HCID 12348 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 1-(Piperidin-1-yl)ethanol | HCID 3030541 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-(2-Piperidinoethoxy)benzoic acid hydrochloride | HCID 5743835 | 68.1% |
반응 단계
Into a 500 ml round bottom flask is placed 23.38 g (197 mmol) of thionyl chloride and 140 ml of methylene chloride. The resulting solution is cooled with an ice bath as 21.91 g (170 mmol) of 1-piperidinoethanol in 30 ml of methylene chloride is added over 30 minutes. After the addition is complete, the ice bath is removed and the mixture is stirred for about 12 hours. The reaction mixture is concentrated on a rotary evaporator to yield a solid residue. Amyl acetate (225 ml), potassium carbonate (34.4 g, 249 mmol), and methyl 4-hydroxybenzoate (14.1 g, 92 mmol) are added to the residue. The resulting slurry is heated to 135° C. for 5 hours. The reaction mixture is cooled to room temperature and washed twice with 100 ml of water. The organic layer is extracted with 53 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 50 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 17.9 g of product, (67%). 1H NMR. Compares to reference solution: HPLC potency 97.9%, TRS 1.50% .
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-b39922028e7646dc804bf6a6f1016d27 |
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| 출처 메모 | uspto-grants-2000_06 |
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