HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromoheptane → 1-Bromo-4-(heptylsulfanyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromoheptane | HCID 12369 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Bromothiophenol | HCID 66049 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Bromo-4-(heptylsulfanyl)benzene | HCID 12521245 | 85% |
Reaction Steps
4-Bromothiophenol (15 g, 0.0794 m) was stirred and heated at 80° C. for 18 hours with n-heptylbromide (14.9 g, 0.0833 m) sodium hydroxide (3.3 g, 0.0833 m) and water (15 mls). The mixture was then added to water (50 mls) and extracted with petroleum spirit 400°-60° (3×50 mls). The combined organic phase was dried over magnesium sulphate and evaporated to yield 4-n-heptylthiobromobonzene (19.5 g, 89% GLC, 85% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05498366 |
| Source dataset | uspto-grants-1996_03 |
| ORD ID | ord-90f208201df14bc297a8ea2669b3cb29 |
| Source note | uspto-grants-1996_03 |