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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53608생성일: 2026년 10월 23일

4-Methoxybenzyl alcohol → 4-Methoxybenzyl 2-bromoacetate

https://huagongshe.com/ko/reaction/53608

반응식

참여 물질

역할이름HCID투입량
반응물4-Methoxybenzyl alcoholHCID 7738—
반응물TriethylamineHCID 8471—
반응물Bromoacetyl bromideHCID 61147—
용매DichloromethaneHCID 6344—
생성물4-Methoxybenzyl 2-bromoacetateHCID 1323323493%

반응 단계

To a -78° C. solution of p-methoxybenzyl alcohol (6.91 g, 50 mmol) and triethylamine (6.95 mL, 50 mmol) in anhydrous CH2Cl2 (50 mL) was added a solution of bromoacetyl bromide (10.1 g, 50 mmol) in CH2Cl2 at -78° C. under nitrogen, over a period of 10 min. The cooling bath was removed, and the reaction mixture was stirred for 2 h. The mixture was washed with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated to provide 12 g (93% yield) of p-methoxybenzyl bromoacetate as a dark colored oil which was used in the next reaction without purification. A portion was purified by column chromatography on silica gel (elution with 20% ethyl acetate/hexanes) to give a clear, colorless oil. 1H NMR (300 MHz, CDCl3) δ3.79 (s, 3H), 3.83 (s, 2H), 5.12 (s, 2H), 6.87 (m, 2H), and 7.30 (m, 2H); IR (film) 1738 cm-1 ; MS (ESI/NH4OAc) M+NH4+ =276.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620969
출처 데이터셋uspto-grants-1997_04
ORD IDord-baef67d864bb431796e9a0a96a3b5860
출처 메모uspto-grants-1997_04