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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493092생성일: 2026년 10월 26일

Tris(propan-2-yl)silanethiol → Methyl-(2-triisopropylsilanylsulfanyl-benzyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/493092

반응식

참여 물질

역할이름HCID투입량
반응물Tris(propan-2-yl)silanethiolHCID 3435097—
반응물Sodium t-butoxideHCID 23676156—
반응물tert-Butyl 2-iodobenzyl(methyl)carbamateHCID 67018447—
촉매Bis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물Methyl-(2-triisopropylsilanylsulfanyl-benzyl)-carbamic acid tert-butyl esterHCID 67018449387%

반응 조건

온도160 °C

반응 단계

(2-Iodo-benzyl)-methyl-carbamic acid tert-butyl ester (3.0 g, 8.64 mmol), tris(dibenzylideneacetone)dipalladium (0) (79 mg, 0.086 mmol), bis(2-diphenylphosphinophenyl)ether (93 mg, 0.17 mmol), sodium tert-butoxide (1.10 g, 11.2 mmol), triisopropylsilanethiol (1.73 g, 9.07 mmol) and dry toluene (15 mL) are all placed in an Emrys Optimizer EXP 20 mL microwave reactor tube. The reaction vessel is sealed and subjected to microwave heating at 160° C. for 15 minutes. Upon cooling the mixture is poured onto a plug of silica and the product is eluted with ethyl acetate-heptane (1:4). This procedure is repeated an additional 3 times to furnish a total of 13.7 g (97%) of the title compound as an oil which is used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534791B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-b2416be841294e798e23e6aab34f8d16
출처 메모uspto-grants-2009_05