HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19727Generated: October 26, 2026
Water → 2-(2-Methoxymethylindan-2-yl)-isoindole-1,3-dione
https://huagongshe.com/reaction/19727
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 2-(2-Hydroxymethylindan-2-yl)-isoindole-1,3-dione | HCID 68561206 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-Methoxymethylindan-2-yl)-isoindole-1,3-dione | HCID 68563231 | — |
Reaction Steps
(Trimethylsilyl)diazomethane (2 M hexanes, 0.51 ml, 1.03 mmol) is added dropwise to a cooled (0° C.) solution of 2-(2-hydroxymethylindan-2-yl)-isoindole-1,3-dione (0.150 g, 0.511 mmol) and fluoroboric acid (48% aqueous, 93.5 μl, 0.511 mmol) in CH2Cl2 (4 ml). The reaction is stirred for 20 minutes, then three further portions of (trimethylsilyl)diazomethane (2 M hexanes, 0.128 ml, 0.25 mmol; 64 μl, 0.12 mol; 64 μl, 0.12 mmol)) are made at 20 minute intervals. The reaction is stirred for a further 40 minutes after the final addition, poured into water and extracted with dichloromethane. The organic phase is washed with brine, dried (MgSO4) and evaporated. The crude product is purified by flash chromatography (CH2Cl2 elution) to afford 2-(2-methoxymethylindan-2-yl)-isoindole-1,3-dione, MH+308.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745462B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-ccfc1df5cea4484292ac30f4648842d3 |
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| Source note | uspto-grants-2010_06 |
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