HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757774Generated: October 28, 2026
Benzyl Alcohol → 3,5-Bis(decyloxy)phenylcarbamic acid phenylmethyl ester
https://huagongshe.com/reaction/1757774
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Benzoic acid, 3,5-bis(decyloxy)- | HCID 10320747 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3,5-Bis(decyloxy)phenylcarbamic acid phenylmethyl ester | HCID 9984762 | 79% |
Reaction Steps
To a stirred, ice bath cooled solution of 5.0 g (0.0115 mol) of 3,5-bis(decyloxy)benzoic acid in 100 ml of anhydrous toluene was added dropwise 3.0 ml (0.0138 mol) of diphenylphosphoryl azide followed by dropwise addition of 1.9 ml (0.0138 mol) of triethylamine. The reaction mixture was stirred in the ice bath for 75 minutes and then was heated at 90° for 2 hours. Benzyl alcohol (100 ml) was added and the solutionwas stirred and heated at 90° for 3.5 hours. The solvent was removedunder reduced pressure and most of the excess benzyl alcohol was removed at80°/0.1 mm. Sodium bicarbonate solution (100 ml) was added to the residue and the product was extracted with ethyl acetate. The dried extract was concentrated at reduced pressure to an oil which was purified by HPLC using 25% hexane-ethyl acetate to give 4.87 g (79% yield) of 3,5-bis(decyloxy)phenylcarbamic acid phenylmethyl ester as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05446189 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-6c62fb21bf2c41e9b4bf4a13f7d22241 |
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| Source note | uspto-grants-1995_08 |
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