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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133436생성일: 2026년 10월 26일

3-Fluorophenylacetic acid → Methyl 3-fluorophenylacetate

https://huagongshe.com/reaction/133436

반응식

참여 물질

역할이름HCID투입량
반응물3-Fluorophenylacetic acidHCID 67617—
반응물TrimethylsilyldiazomethaneHCID 167693—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물Methyl 3-fluorophenylacetateHCID 2734108104.1%

반응 단계

To a solution of 3-fluorophenylacetic acid (5.0 g, 32 mmol) in MeOH (25 mL) and CH2Cl2 (25 mL) at 0° C. was added trimethylsilyldiazomethane (2 M in hexane, 30 mL, 60 mmol). After stirring at room temperature for 15 min, the reaction mixture was concentrated to dryness, and the residue was azeotroped with toluene to give the crude methyl 3-fluorophenylacetate (5.6 g), which was used without further purification. Thus, the crude methyl 3-fluorophenylacetate obtained above (2.5 g, 15 mmol) was converted to the title compound (purified on silica gel) by reacting with 4-chlorobenzyl bromide (4.6 g, 22 mmol) and sodium hexamethyldisilazide (1 M in THF, 15 mL, 15 mmol) following the procedure described in Reference Example 10, Step A. 1H NMR (400 MHz, CD3OD): δ 7.35-6.88 (m, 8H), 3.92 (t, 1H), 3.60 (s, 3H), 3.34 (dd, 1H), 3.00 (dd, 1H). LC-MS: m/e 305 (M+Na)+ (3.9 min).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390835B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-95e761487ce846a69929b01fdf4f867b
출처 메모uspto-grants-2008_06