Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339314생성일: 2026년 10월 26일
Tris(hydroxymethyl)aminomethane → N-(2,3-dimethylcyclohexyl)benzo[d][1,3]dioxole-5-carboxamide
https://huagongshe.com/reaction/339314
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| 반응물 | 1,3-Benzodioxole-5-carboxylic acid | HCID 7196 | — |
| 반응물 | 2,3-Dimethylcyclohexylamine | HCID 123507 | — |
| 반응물 | Carbodiimide | HCID 160435 | — |
| 반응물 | HCID 178418300 | HCID 178418300 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Acetonitrile methylene chloride | HCID 21877088 | — |
| 생성물 | N-(2,3-dimethylcyclohexyl)benzo[d][1,3]dioxole-5-carboxamide | HCID 17479454 | — |
반응 단계
2,3-dimethylcyclohexanamine (20 μmol) and benzo[d][1,3]dioxole-5-carboxylic acid (1.1 eq) were each dissolved in acetonitrile/dichloromethane (200 μL, 2:1). PS-Carbodiimide resin (2 eq) was loaded into a 1.2 mL 96 well Greiner plate, followed by the addition of amine and acid solutions. Hydroxybenzotriazole (1.1 eq) was dissolved in DMF (100 mL) and was added into the reaction well. The reaction was shaken overnight at room temperature. Once the reaction was completed, PS-Trisamine resin (1.5 eq) was added into the reaction mixture and the solution was allowed to shake overnight at room temperature. Acetonitrile (200 mL) was added into the reaction well, and the top clear solution was transferred into a new plate. The solution was evaporated to give N-(2,3-dimethylcyclohexyl)benzo[d][1,3]dioxole-5-carboxamide. MS (M+H, 276.20).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08895050B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-214d46e93fd848efac87ce532459a3b5 |
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| 출처 메모 | uspto-grants-2014_11 |
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