HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → phenylmethyl (2-methyl-2,3-dihydro-1H-inden-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| 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 | — |
| Product | phenylmethyl (2-methyl-2,3-dihydro-1H-inden-2-yl)carbamate | HCID 57585915 | 84.5% |
Reaction Steps
To a solution 2-methyl-2,3-dihydro-1H-indene-2-carboxylic acid (0.200 g, 1.14 mmol) and triethylamine (0.166 mL, 1.19 mmol) in 2 mL of benzene at to 0 degrees Centigrade was added diphenyl phosphorylazide (0.257 g, 1.19 mmol). The reaction mixture was stirred for 15 minutes and benzyl alcohol (0.123 mL, 1.19 mmol) was added and the reaction was heated to reflux for 16 hours, then cooled and 10% HCl was added. The organics were extracted 2×25 mL ethyl acetate, then washed 1× brine, dried (Na2SO4), filtered and concentrated. The residue was chromatographed on silica using 5:1 hexanes/ethyl acetate to give 0.271 g of the phenylmethyl (2-methyl-2,3-dihydro-1H-inden-2-yl)carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939528B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-8c8181c7c4ff4b5db6d0d37b1bd0c091 |
| Source note | uspto-grants-2011_05 |