Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 266093생성일: 2026년 10월 26일
Methane → alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-phenyl-2-benzothiazolemethanol
https://huagongshe.com/reaction/266093
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methane | HCID 297 | — |
| 반응물 | [2-Benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl)methanone | HCID 9842862 | — |
| 반응물 | HCID 178506676 | HCID 178506676 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Cyclohexane diethylether | HCID 21895417 | — |
| 생성물 | alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-phenyl-2-benzothiazolemethanol | HCID 18930344 | — |
반응 단계
Dissolve [2-benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]methanone (2.0 g, 5.26 mmol) in anhydrous tetrahydrofuran (50 mL), place under an argon atmosphere and cool to -78° C. Add, by dropwise addition, phenyllithium (3.16 mL of a 2.0M solution in cyclohexane/ethyl ether, 6.31 mmol). Stir at -78° C. for 30 minutes, quench with saturated ammonium chloride (100 mL), separate the organic phase and extract the aqueous phase with ethyl acetate. Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo. Purify by chromatography (75% ethyl acetate/hexane) to give a yellow oil. Dissolve the oil in methylene chloride and treat with activated charcoal.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05650416 |
|---|
| 출처 데이터셋 | uspto-grants-1997_07 |
|---|
| ORD ID | ord-89916258f28a42408349c04189ac3716 |
|---|
| 출처 메모 | uspto-grants-1997_07 |
|---|