HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82879Generated: October 30, 2026
HCID 66741339, compound → ethyl 1-benzyl-1-hydroxy-6-methoxy-2,3-dihydro-1H-inden-2-ylcarbamate
https://huagongshe.com/reaction/82879
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 66741339 | HCID 66741339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 1-benzyl-1-hydroxy-6-methoxy-2,3-dihydro-1H-inden-2-ylcarbamate | HCID 66741247 | — |
Reaction Steps
To ice cold 2M benzylmagnesium chloride in tetrahydrofuran (6.14 ml, 12.28 mmol) was added dropwise a solution of ethyl 6-methoxy-1-oxo-2,3-dihydro-1H-inden-2-ylcarbamate (1.02 g. 4.09 mmol) in tetrahydrofuran (30 ml) and stirred over night, while the reaction mixture was allowed to warm up to room temperature. The reaction mixture was quenched with sat. ammonium chloride and the organic layer was evaporated. The residue was extracted twice with dichloromethane and the combined organic layers were washed subsequently with sodium bicarbonate and brine, dried, filtered and evaporated to obtain a dark gooey oil, that was purified by flash silica gel chromatography on 12 g SiO2-cartridge using 30% ethyl acetate in cyclohexane to afford the desired ethyl 1-benzyl-1-hydroxy-6-methoxy-2,3-dihydro-1H-inden-2-ylcarbamate as a brown grease. m=1.07 g (77%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846743B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-f4eb8fbeed024531a34cbb0d023de8c4 |
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| Source note | uspto-grants-2014_09 |
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