HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70280Generated: October 28, 2026
Benzyl Alcohol → phenylmethyl (2-methyl-2,3-dihydro-1H-inden-2-yl)carbamate
https://huagongshe.com/reaction/70280
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 2-methyl-2,3-dihydro-1H-indene-2-carboxylic acid | HCID 15338842 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | phenylmethyl (2-methyl-2,3-dihydro-1H-inden-2-yl)carbamate | HCID 57585915 | — |
Reaction Steps
To a solution of 2-methyl-2,3-dihydro-1H-indene-2-carboxylic acid (0.200 g, 1.14 mmol) and triethylamine (0.17 mL, 1.2 mmol) in benzene (2 mL) at 0° C. was added diphenyl phosphorylazide (0.257 g, 1.19 mmol). The mixture was stirred 15 min, benzyl alcohol (0.123 mL, 1.19 mmol) was added and the reaction was heated under reflux for 16 hours. Upon cooling, the mixture was diluted with 10% HCl and extracted with ethyl acetate (2×25 mL). Combined organics were washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography (EtOAc/hexanes) affording the title compound. 1H NMR (400 MHz, CDCl3) δ ppm 1.55 (s, 3H), 2.98 (d, J=15.9 Hz, 2 H), 3.28 (d, J=15.9 Hz, 2 H), 7.12-7.18 (m, 4H), 7.29-7.37 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822518B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-91c6aeb92dcd44c79a8a6341eb4ee6ec |
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| Source note | uspto-grants-2014_09 |
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