HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 7-Bromo-4,4-dimethylthiochroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | m-Bromophenyl 3-methyl-2-butenyl sulfide | HCID 22640690 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-Bromo-4,4-dimethylthiochroman | HCID 22393099 | 86.6% |
Reaction Steps
A solution of 1-bromo-3-(3-methyl-but-2-enylsulfanyl)-benzene (5.651 g, 22 mmole) in 100 mL of toluene was treated with 5.433 g of p-toluenesulfonic acid monohydrate and heated at reflux for 15 hours. The mixture was diluted with 100 mL of water, neutralized with solid sodium bicarbonate and extracted with two 100 mL portions of ethyl acetate. The organic phase was dried over MgSO4, filtered and concentrated in vacuo to give a yellow oil. The product was purified by short path distillation (T=190° C. at 1.08 Torr) to give 4.902 g of 7-bromo-4,4-dimethyl-thiochroman as a pale yellow oil, which contained approximately 20% 5-bromo-4,4-dimethyl-thiochroman.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07354931B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-7f5874c302d1406197f2a223c30302c2 |
| Source note | uspto-grants-2008_04 |