Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Chloroethanol → 4-(2-chloroethoxy)-1H-indole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Chloroethanol | HCID 34 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 1H-indol-4-ol | HCID 75421 | — |
| 반응물 | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Diethylether hexane | HCID 21584099 | — |
| 생성물 | 4-(2-chloroethoxy)-1H-indole | HCID 10631721 | — |
반응 단계
A solution of 4-hydroxyindole (3.99 g, 30 mmol), 2-chloroethanol (6.03 ml, 90 mmol) and triphenylphosphine (23.6 g, 90 mmol) in tetrahydrofuran is treated with diethyl azodicarboxylate (14.1 ml, 90 mmol) under nitrogen at room temperature, stirred for 2 hr at room temperature and concentrated in vacuo to give a residue. Cooled diethyl ether is added to the residue and the solid triphenylphosphine oxide is precipitated and removed by filtration. The filtrate is concentrated and purified by flash chromatography (silica gel, EtOAc/hexane: 1.5/8.5) to give an oil. After trituration with Et2O/hexane (1/10), the title compound is obtained as a white solid, 4.8 g (82%) mp 60° C., identified by NMR and mass spectral analyses.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06710069B2 |
| 출처 데이터셋 | uspto-grants-2004_03 |
| ORD ID | ord-af2ab9939a1c410482122c231543542d |
| 출처 메모 | uspto-grants-2004_03 |