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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32970생성일: 2026년 10월 25일

Diisopropyl bromomethylphosphonate → {2-[6-Methoxy-7-methyl-3-oxo-4-(2-trimethylsilany-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-ethoxymethyl}-phosphonic Acid Diisopropyl Ester

https://huagongshe.com/reaction/32970

반응식

참여 물질

역할이름HCID투입량
반응물Diisopropyl bromomethylphosphonateHCID 4366885—
반응물2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
반응물6-(2-Hydroxy-ethyl)-5-methoxy-4-methyl-7-(2-trimethylsilanyl-ethoxy)-3H-isobenzofuran-1-oneHCID 57459851—
용매DimethylformamideHCID 6228—
생성물{2-[6-Methoxy-7-methyl-3-oxo-4-(2-trimethylsilany-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-ethoxymethyl}-phosphonic Acid Diisopropyl EsterHCID 57478687—

반응 단계

A mixture of 6-(2-hydroxy-ethyl)-5-methoxy-4-methyl-7-(2-trimethylsilanyl-ethoxy)-3H-isobenzofuran-1-one (79 mg, 0.23 mmol) was heated with bromomethylphosphonic acid diisopropyl ester (120 mg, 0.46 mmol) in the presence of lithium t-butoxide (22 mg, 0.27 mmol) in DMF (2 mL) at 70° C. overnight. The reaction mixture was purified by RP HPLC (acetonitrile and 0.1% aqueous CF3COOH) to provide the desired product. 1H NMR (300 MHz, CDCl3) δ 0.00 (s, 9H), 1.13-1.25 (m, 2H), 1.26 (t, 12H, J=6 Hz), 2.12 (s, 3H), 2.98 (t, 2H, J=7 Hz), 3.60-3.73 (m, 4H), 3.77 (s, 3H), 4.05-4.16 (m, 2H), 4.62-4.74 (m, 2H), 5.07 (s, 2H) ppm; MS (m/z) 539 [M+Na]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427636B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-82327874a61b4984839a6e402c5c2154
출처 메모uspto-grants-2008_09