Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70497생성일: 2026년 10월 25일
Ammonium Chloride → (5-Chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanol
https://huagongshe.com/reaction/70497
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 4-Bromothioanisole | HCID 66037 | — |
| 반응물 | 5-Chloro-6-methoxypicolinaldehyde | HCID 58452846 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (5-Chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanol | HCID 67396108 | 72.3% |
반응 단계
n-Butyllithium (2.64 M, 2.9 mL) was added to a solution of 4-bromothioanisole (1.61 g) in tetrahydrofuran (20 mL) at −78° C. in a nitrogen atmosphere, and the mixture was stirred at the same temperature for 30 minutes. A solution of 5-chloro-6-methoxypyridine-2-carbaldehyde (1.14 g) in tetrahydrofuran (10 mL) was added to the reaction solution, followed by stirring for one hour. The reaction solution was poured into a saturated ammonium chloride solution, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered, after which the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1→4:1) to give (5-chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanol as a pale yellow oil (1.42 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08822503B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_09 |
|---|
| ORD ID | ord-f806ee9f51c84a7e8397092246675d0c |
|---|
| 출처 메모 | uspto-grants-2014_09 |
|---|