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HRID 46312생성일: 2026년 10월 24일

Chlorotrimethylsilane → tert-Butyl3-(2-{[tert-butyl(dimethyl)silyl]oxy)-5-chlorophenyl)azetidine-1-carboxylate

https://huagongshe.com/ko/reaction/46312

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참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물1,2-DibromoethaneHCID 7839—
반응물Tris(furan-2-yl)phosphaneHCID 521585—
반응물Tert-butyl 3-iodoazetidine-1-carboxylateHCID 11000522—
반응물Tert-butyl(4-chloro-2-iodophenoxy)dimethylsilaneHCID 59436493—
촉매ZincHCID 23994—
촉매(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one palladiumHCID 15673654—
용매DimethylformamideHCID 6228—
생성물tert-Butyl3-(2-{[tert-butyl(dimethyl)silyl]oxy)-5-chlorophenyl)azetidine-1-carboxylateHCID 59436503—

반응 조건

온도60 °C

반응 단계

Zinc powder (700 mg, 10.7 mmol) was suspended in N,N-dimethylformamide (20 ml) under nitrogen. 1,2-dibromoethane (120 ul) was added and suspension heated to 60° C. for 10 minutes before cooling to room temperature. Chlorotrimethylsilane (180 ul) was added and the mixture heated to 60° C. for 10 minutes then cooled to room temperature. tert-Butyl 3-iodoazetidine-1-carboxylate (3.0 g, 10.6 mmol) was added with a slight exotherm observed. The mixture was stirred at room temperature for 1 hour before the addition of tert-butyl(4-chloro-2-iodophenoxy)dimethylsilane (Preparation 239, 2.2 g, 5.97 mmol) followed immediately by tri-2-furylphosphine (250 mg, 1.08 mmol) and (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one-palladium (2:1) (300 mg, 0.52 mmol). The mixture was stirred at room temperature for 30 minutes then heated at 70° C. for 5 hours before concentration in vacuo. The residue was partitioned between ethyl acetate (100 ml) and aqueous sodium carbonate solution (50 ml). The organic extract was dried over sodium sulphate, filtered and evaporated in vacuo to afford the title compound as a brown oil, 3.2 g,

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541588B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-44909872de054f04a9baddf64ddcecc0
출처 메모uspto-grants-2013_09