HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910509Generated: October 29, 2026
2,6-Lutidine → [2-(4-Hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-isobenzofuran-5-yl)-ethoxymethyl]-phosphonic Acid
https://huagongshe.com/reaction/910509
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | {2-[6-Methoxy-7-methyl-3-oxo-4-(2-trimethylsilany-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-ethoxymethyl}-phosphonic Acid Diisopropyl Ester | HCID 57478687 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [2-(4-Hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-isobenzofuran-5-yl)-ethoxymethyl]-phosphonic Acid | HCID 59794464 | — |
Reaction Steps
To a solution of {2-[6-methoxy-7-methyl-3-oxo-4-(2-trimethylsilanyl-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-ethoxymethyl}-phosphonic acid diisopropyl ester (7.5 mg, 0.014 mmol) in acetonitrile (2 mL) and 2,6-lutidine (25 μL, 0.21 mmol) was added trimethylsilyl bromide (27 μL, 0.21 mmol) at room temperature. The reaction was allowed to proceed for 18 hours when completion of the reaction was indicated by LCMS. The reaction was quenched by addition of MeOH and concentration. The residue was purified by RP-HPLC using a C18 column. The collected product was dissolved in a solution of 10% TFA/CH2Cl2 to assure complete deprotection. The reaction mixture was lyophilized to provide the desired product. 1H NMR (300 MHz, CD3OD) δ 2.12 (s, 3H), 2.98 (t, 2H, J=7 Hz), 3.66-3.76 (m, 4H), 3.78 (s, 3H), 5.21 (s, 2H) ppm; MS (m/z) 331 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022083B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-fac4412b9e3e44eea05793dd463da918 |
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| Source note | uspto-grants-2011_09 |
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