HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl Isothiocyanate → Phenylthiocarbamic acid O-(4-hydroxymethyl-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepin-4-ylmethyl) ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl Isothiocyanate | HCID 7673 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,4-Bis(hydroxymethyl)-3,4-dihydro-2H-benzo[b]oxepin-5-one | HCID 67073125 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phenylthiocarbamic acid O-(4-hydroxymethyl-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepin-4-ylmethyl) ester | HCID 86633681 | — |
Reaction Steps
To a solution of 4,4-bis(hydroxymethyl)-3,4-dihydro-2H-benzo[b]oxepin-5-one (500 mg, 2.25 mmol) in 28 ml of tetrahydrofuran were added, at room temperature, triethylamine (0.34 ml, 2.5 mmol) and phenyl isothiocyanate (672 μl, 5.63 mmol). The mixture was heated to reflux for 72 hours, concentrated and purified by column chromatography on silica gel (eluent: 1:1 tert-butyl methyl ether/cyclohexane). The product was obtained in a yield of 149 mg (19%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858613B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-8aa5679a085849e1927ce31a861e643f |
| Source note | uspto-grants-2010_12 |