HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274025Generated: October 27, 2026
Benzeneacetic acid, 3,4-dimethoxy-, methyl ester → alpha-[5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]pentyl]-3,4-dimethoxybenzeneacetic acid methyl ester
https://huagongshe.com/reaction/274025
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzeneacetic acid, 3,4-dimethoxy-, methyl ester | HCID 85213 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2,3-dihydro-6-methoxy-1H-isoindol-5-ol | HCID 10241135 | — |
| Reactant | (5-Bromopentyl)(1,1-dimethylethyl)dimethyl silane | HCID 19042078 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | alpha-[5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]pentyl]-3,4-dimethoxybenzeneacetic acid methyl ester | HCID 54212729 | — |
Reaction Steps
To a solution, -78° C. under argon, of 2 38 g of 3,4-dimethoxyphenyl acetic acid methyl ester in 30 ml of tetrahydrofuran is added 12.45 ml of 1.0M sodium hexamethylsidilazide. The solution is stirred at -78° C. for 5 minutes and then warmed to 0° C. for 1 hour. To this solution is added 3.5 g of (5-bromopentyl)(1,1-dimethylethyl)dimethyl silane. The reaction mixture is allowed to warm to room temperature and stirred for 12 hours. The mixture is diluted with diethyl ether and water, the layers are separated and the organic layer is washed with saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by chromatography (silica gel: hexane/ethyl acetate,5/1) to give 2.6 g of the desired product as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05387685 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-278b8b799112408cad48b628991a6464 |
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| Source note | uspto-grants-1995_02 |
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