Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 854242생성일: 2026년 10월 27일
Tributylphosphine → 6-(3-Piperidin-1-yl-propoxy)-naphthalene-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/854242
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tributylphosphine | HCID 13831 | — |
| 반응물 | Piperidine-1-propanol | HCID 66032 | — |
| 반응물 | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| 반응물 | Methyl 6-hydroxy-2-naphthoate | HCID 390995 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6-(3-Piperidin-1-yl-propoxy)-naphthalene-2-carboxylic acid methyl ester | HCID 58933893 | 76.4% |
반응 단계
A mixture of 20.2 g (0.1 mol) 6-hydroxy-naphthalene-2-carboxylic acid methyl ester (commercially available), 18.6 g (0.13 mol) 1-piperidinepropanol (commercially available), 50.4 g (0.2 mol) 1,1′-(azodicarbonyl)dipiperidine and 58 ml (0.2 mol) tri-n-butyl-phosphine in 400 ml THF was stirred at room temperature for 16 h. The suspension was filtered off and the filtrate evaoprated to dryness. The residue was taken up in 200 ml DCM and 400 g Isolute® HM-N (Argonaut Technologies Inc., support material for accelerated solvent extraction) was added and evaporated to dryness. The residue was chromatographed over silica eluting with a gradient formed from DCM/MeOH(2N NH3) 99/1 to 9/1. After evaporation the residue was treated with heptan/diethyl ether and the precipitate filtered of and washed again with heptan/diethyl ether. After drying under reduced pressure at 50° C. 25 g (76%) of the title compound was obtained as white solid. MS (m/e): 328.3 (MH+, 100%)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07259158B2 |
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| 출처 데이터셋 | uspto-grants-2007_08 |
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| ORD ID | ord-02f4c9ea89154cd09ef829f9f0a3a884 |
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| 출처 메모 | uspto-grants-2007_08 |
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