HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → [4-(Prop-2-en-1-yloxy)phenyl]methanethiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 1-Allyloxy-4-chloromethyl-benzene | HCID 12347936 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [4-(Prop-2-en-1-yloxy)phenyl]methanethiol | HCID 22242087 | 81% |
Reaction Steps
A mixture of 2.00 g (10.9 mmol) 1-allyloxy-4-chloromethyl-benzene and 917 mg (12.1 mmol) thiourea in 3.0 ml ethanol was heated to reflux for 7 h. Solvents were distilled off and the crystalline residue was washed with cold ethanol and isolated by filtration. After addition of 2.5 ml ethanol, 1.0 ml water and 0.7 ml 25% aqueous ammonia, the mixture was heated to reflux for 1 h. Ethanol was distilled off, then acidified with 0.5 ml half conc. HCl and extracted with ethyl acetate. The solution was dried over MgSO4 and solvents were removed in vacuo to yield 1.59 g (81%) colorless oil, which was used immediately.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07429605B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-70d7487da8084e27bd9cb2a255ecb9de |
| Source note | uspto-grants-2008_09 |