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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 991431생성일: 2026년 10월 27일

O-Xylene → Phthalazine

https://huagongshe.com/reaction/991431

반응식

참여 물질

역할이름HCID투입량
반응물O-XyleneHCID 7237—
반응물Triethylamine hydrochlorideHCID 11130—
반응물NitrosamineHCID 37183—
생성물PhthalazineHCID 920763%

반응 단계

1,1′-Carbonyldiimidazole (2.0 g, 12.6 mmol) was added to a stirred solution of 5-methylisoxazole-3-carboxylic acid in DMF (50 ml). The solution was stirred for 0.5 h before adding the preceding hydrazine (2.63 g, 11.7 mmol). After 1 h at room temperature, the solution was poured into water and the resultant precipitate was filtered, washed with water (30 ml) and hexane (100 ml), and dried in vacuo to give the ketohydrazine (3.1 g, 79%); MS (ES+) m/e 334 [MH]+. A solution of the ketohydrazine (1.0 g, 3.0 mmol) and triethylamine hydrochloride (0.2 g, 1.45 mmol), in xylene (30 ml), was heated at reflux for 4 h. The solution was cooled to room temperature and the solvent removed in vacuo. The residue was chromatographed through silica gel, eluting with ethyl acetate, to give the title-phthalazine (0.60 g, 63%), mp 186-188° C.; 1H NMR (250 MHz, CDCl3) δ1.22-1.54 (4H, m, 2 of CH2), 1.94-2.06 (4H, m, 2 of CH2), 2.58 (3H, s, Me), 3.60 (1H, s, CH), 4.08 (1H, s, CH), 6.90 (1H, s, Ar—H); MS (ES+) m/e 316 [MH]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06465462B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-9913f1aeaf764cccafb8ed6d9df03066
출처 메모uspto-grants-2002_10