Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 2-((Benzyloxy)methyl)-1,3-dioxane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1,3-Propanediol | HCID 10442 | — |
| 반응물 | Ethyl orthoformate | HCID 31214 | — |
| 반응물 | (Phenylmethoxy)acetaldehyde | HCID 108989 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 생성물 | 2-((Benzyloxy)methyl)-1,3-dioxane | HCID 59792378 | 58% |
반응 단계
A mixture of benzyloxyacetaldehyde (3.6 g, 24 mmol), 1,3-propanediol (5.2 ml, 72 mmol), triethyl orthoformate (4 ml, 24 mmol), and p-toluenesulfonic acid monohydrate (414 mg, 2.45 mmol) was stirred at room temperature for 17 hours. To the reaction mixture, triethylamine (669 μl, 4.8 mmol) was added, which was concentrated. The residue was purified by silica gel column chromatography (elution solvent: heptane/ethyl acetate) to obtain the title compound (2.9 g, yield: 58%) as a light yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07425634B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-9f39e15806ee44feb5cf00cee9492e0e |
| 출처 메모 | uspto-grants-2008_09 |