HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654939Generated: October 30, 2026
Benzyl Alcohol → 2-(Benzyloxycarbonylaminomethyl)indan
https://huagongshe.com/reaction/1654939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 2-(2,3-dihydro-1H-inden-2-yl)acetic Acid | HCID 5174955 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(Benzyloxycarbonylaminomethyl)indan | HCID 18921483 | 86.4% |
Reaction Steps
17.6 g (0.10 mol) of (indan-2-yl)acetic acid was dissolved in 150 ml of toluene, to which were added 15.3 ml (0.11 mol) of triethylamine and 33.0 g (0.12 mol) of diphenylphosphorylazide, and stirred at room temperature for 30 minutes. The mixture was added with 16.6 g (0.15 mol) of benzyl alcohol and refluxed for 18 hours. After cooling, the solvent was distilled under reduced pressure, and the residue was added with 500 ml of ethyl acetate, washed with 1N sodium hydroxide, and condensed. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:3), and the crystals collected were recrystallized from a solvent mixture of ethyl acetate and hexane to obtain 24.3 g of 2-(benzyloxycarbonylaminomethyl)indan as colorless needles. Yield: 86%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05409956 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-cdd8da38ea0e4a7daae1763de9468670 |
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| Source note | uspto-grants-1995_04 |
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