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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tris(propan-2-yl)silanethiol | HCID 3435097 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 반응물 | tert-Butyl 2-iodobenzyl(methyl)carbamate | HCID 67018447 | — |
| 촉매 | Bis[2-(diphenylphosphino)phenyl] ether | HCID 4285986 | — |
| 촉매 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Methyl-(2-triisopropylsilanylsulfanyl-benzyl)-carbamic acid tert-butyl ester | HCID 67018449 | 387% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07534791B2 |
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| 출처 데이터셋 | uspto-grants-2009_05 |
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| ORD ID | ord-b2416be841294e798e23e6aab34f8d16 |
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| 출처 메모 | uspto-grants-2009_05 |
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