Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2387708생성일: 2026년 10월 25일
Trimethylsilylacetylene → Methyl-(3-trimethylsilanylethynyl-benzyl)-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/2387708
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trimethylsilylacetylene | HCID 66111 | — |
| 반응물 | tert-Butyl 3-bromobenzyl(methyl)carbamate | HCID 20738487 | — |
| 촉매 | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | Methyl-(3-trimethylsilanylethynyl-benzyl)-carbamic acid tert-butyl ester | HCID 60133802 | — |
반응 단계
TMS-Acetylene (2.2 mL, 15.0 mmol) was added dropwise to commercially available tert-butyl 3-bromobenzyl(methyl)carbamate (3.0 g, 10 mmol), CuI (100 mg, 0.5 mmol) and palladium dichlorobistriphenylphosphine (210 mg, 0.3 mmol) in triethylamine (30 mL) at room temperature under a nitrogen atmosphere. The reaction mixture was heated to 70° C. for 12 hrs before cooling to room temperature and evaporating in vacuo. The residue was triturated with diethyl ether (30 mL), filtered and the filtrate evaporated in vacuo and purified by column chromatography (5% ethyl acetate in hexane) to yield A314.1 (3.2 g, 100%) as a brown oil. HPLC YMC S-5 4.6×33 mm (2 min grad): retention time 2.34 min, M+Na+=340.34
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08268855B2 |
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| 출처 데이터셋 | uspto-grants-2012_09 |
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| ORD ID | ord-013b702c91bc4f508c0d68b0df41921e |
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| 출처 메모 | uspto-grants-2012_09 |
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