HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl isocyanate → 4-Isothiocyanatophenyl butylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | Phenol, 4-isothiocyanato- | HCID 102208 | — |
| Reactant | Di-n-butyldilauryltin | HCID 9809426 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-Isothiocyanatophenyl butylcarbamate | HCID 21489009 | — |
Reaction Steps
Three and eight-tenths grams (3.8 g.) (0.025 m.) of p-hydroxyphenylisothiocyanate was mixed with 2.5 g. (0.025 m.) of n-butylisocyanate in 50 mls. of benzene. To this mixture was added 3 drops each of triethylamine and dibutyltin dilaurate, and the mixture was allowed to stand at ambient temperature over night. After refluxing on the steam-bath for thirty minutes, the solvent was removed under vacuum by means of a rotary evaporator. The residue was slurried in n-hexane, filtered and air dried. There was obtained 5.4 grams of solid, m.p. 99°-102° C. The structure was confirmed by I.R.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04000253 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-d0fa6f81caed4614be214d4a11910119 |
| Source note | uspto-grants-1976_12 |