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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrafluoroboric acidHCID 28118—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant2-(2-Hydroxymethylindan-2-yl)-isoindole-1,3-dioneHCID 68561206—
SolventDichloromethaneHCID 6344—
Product2-(2-Methoxymethylindan-2-yl)-isoindole-1,3-dioneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745462B2
Source datasetuspto-grants-2010_06
ORD IDord-ccfc1df5cea4484292ac30f4648842d3
Source noteuspto-grants-2010_06