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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1168441생성일: 2026년 10월 26일

tert-Butyl methyl ether → Methyl 2-{3-[2-(4-bromophenyl)-5-methyloxazol-4-ylmethoxy]cyclohexyloxymethyl}-6-methylbenzoate

https://huagongshe.com/reaction/1168441

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl methyl etherHCID 15413—
반응물Sodium hydrideHCID 24758—
반응물Methyl 2-(3-hydroxycyclohexyloxymethyl)-6-methylbenzoateHCID 21980299—
반응물2-(4-Bromophenyl)4-iodomethyl-5-methyloxazoleHCID 22493666—
용매DimethylformamideHCID 6228—
생성물Methyl 2-{3-[2-(4-bromophenyl)-5-methyloxazol-4-ylmethoxy]cyclohexyloxymethyl}-6-methylbenzoateHCID 22493646—

반응 단계

At room temperature, 50 mg of a 60% sodium hydride suspension and then 408 mg of 2-(4-bromophenyl)4-iodomethyl-5-methyloxazole were added to a solution of 200 mg of methyl 2-(3-hydroxycyclohexyloxymethyl)-6-methylbenzoate in 5 ml of dimethylformamide. After one hour, methyl tert-butyl ether was added, and the mixture was extracted with water. The organic phase was dried over magnesium sulfate, the solvents were removed under reduced pressure and the residue was purified by RP-HPLC. This gave 49 as a light-yellow oil. C27H30BrNO5 (528.45), MS(ESI): 528.2, 530.2 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06624185B2
출처 데이터셋uspto-grants-2003_09
ORD IDord-51dca3bb666d4701872701851bcad533
출처 메모uspto-grants-2003_09