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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1156682생성일: 2026년 10월 25일

Phenolate Sodium → 3-(1,3-Dimethylcyclobutanecarbonyloxy)-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketone

https://huagongshe.com/reaction/1156682

반응식

참여 물질

역할이름HCID투입량
반응물Phenolate SodiumHCID 4445035—
반응물Sodium MethoxideHCID 10942334—
반응물3-Hydroxy-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketoneHCID 12295018—
반응물1,3-Dimethylcyclobutanecarbonyl chlorideHCID 20535379—
생성물3-(1,3-Dimethylcyclobutanecarbonyloxy)-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketoneHCID 20535395—

반응 단계

Following a procedure similar to that described in Example 13A above, when 3-hydroxy-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketone is interacted with one equivalent of sodium methoxide and the resulting sodium phenolate salt is reacted with 1,3-dimethylcyclobutanecarbonyl chloride there is obtained 3-(1,3-dimethylcyclobutanecarbonyloxy)-4-(isovaleryloxy)-phenyl tert-butylaminomethyl ketone which reacts with hydrochloric acid to yield the hydrochloric salt. When this hydrochloride is catalytically hydrogenated, using the procedure described above in Example 13B, there is obtained 3-(1,3-dimethylcyclobutanecarbonyloxy)-4-(isovaleryloxy)-alpha-(tert-butylaminomethyl)-benzyl alcohol hydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04336400
출처 데이터셋uspto-grants-1982_06
ORD IDord-211613bd4b2b44cfa19f317a82cc5842
출처 메모uspto-grants-1982_06