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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10394생성일: 2026년 10월 24일

Formaldehyde → 5-Bromo-2-benzothiazoleethanol

https://huagongshe.com/ko/reaction/10394

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Ammonium ChlorideHCID 25517—
반응물5-Bromo-2-methylbenzothiazoleHCID 3017457—
반응물ButyllithiumHCID 178418339—
반응물HCID 178418821HCID 178418821—
용매TetrahydrofuranHCID 8028—
생성물5-Bromo-2-benzothiazoleethanolHCID 21980060—

반응 조건

온도-78 °C

반응 단계

To a dry 100 mL flask, 2,2,6′,6′-tetra-methyl piperidine (0.56 g, 4 mmol) and 6 mL of THF was added and cooled to −78° C. Then n-BuLi (1.5 mL, 2.5M) was added rapidly, and the mixture of LiTMP was stirred for 3 hr. 5-Bromo-2-methyl-benzothiazole (0.75 g, 3.3 mmol) was added in solid form in to the reaction at −78° C., and after stirring for 4 hours at −78° C., 6 equivalents of para-formaldehyde was added to the reaction while stirring rapidly. The reaction was worked up by addition of sat. NH4Cl solution, and the reaction was extracted with CH2Cl2 dried, and concentrated in vacuo to give crude product, 1.02 g. The crude product was purified by flash chromatography, eluting with CH2Cl2, then with 20% MeOH/CH2Cl2 to elute the product. 1H NMR (400 MHz, CDCl3) d ppm 3.32 (t, J=5.76 Hz, 2 H) 4.11 (q, J=5.95 Hz, 2 H) 7.48 (dd, J=8.51, 1.92 Hz, 1 H) 7.70 (d, J=8.51 Hz, 1 H) 8.11 (d, J=1.92 Hz, 1 H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094790B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-1090695690f74685a1dece36db0314be
출처 메모uspto-grants-2006_08