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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1488661생성일: 2026년 10월 25일

3-Nitrobenzoic acid → Biphenyl indolizinyl nitrobenzoate

https://huagongshe.com/reaction/1488661

반응식

참여 물질

역할이름HCID투입량
반응물3-Nitrobenzoic acidHCID 8497—
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물HCID 178516797HCID 178516797—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Biphenyl indolizinyl nitrobenzoateHCID 86748744—

반응 단계

Alternatively, the biphenyl trans-hydroxy triazole can be prepared using the Mitsunobu reaction conditions. To a solution of diethyl azodicarboxylate (2.0 mmol) and 3-nitrobenzoic acid (2.0 mmol) in 2.0 mL of THF is added dropwise a solution of the biphenyl hydroxy triazole (2.0 mmol, obtained from Step 1 of Example 3261), and triphenylphosphine (2.0 mmol) in 1.0 mL of THF at room temperature. The resulting solution is stirred at room temperature until the reaction is complete. The resulting mixture is diluted with ether or ethyl acetate, and washed with water. The extracts are dried (MgSO4) and concentrated in vacuo to give the biphenyl indolizinyl nitrobenzoate. The crude benzoate is hydrolyzed with LiOH in aqueous THF at room temperture and purified to give the biphenyl trans-hydroxy triazole.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05674879
출처 데이터셋uspto-grants-1997_10
ORD IDord-cdc9140e847047f980fa018cf359010f
출처 메모uspto-grants-1997_10