HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → methyl 5-tert-butylfuran-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | t-Butyl bromide | HCID 10485 | — |
| Reactant | Methyl 2-furoate | HCID 11902 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | methyl 5-tert-butylfuran-2-carboxylate | HCID 250082 | — |
Reaction Steps
AlCl3 (25.4 g, 190 mmol) is added batchwise to methyl furan-2-carboxylate (20.0 g, 159 mmol) and tert.-butylbromide (21.4 mL, 190 mmol) in CS2 (200 mL) while cooling with ice and the mixture is stirred for 6 h at RT. The reaction mixture is poured onto ice water, mixed with conc. hydrochloric acid (25 mL) and stirred for 10 min. Then the aqueous phase is extracted 2× with 200 mL EA. The combined organic phase is dried on Na2SO4, filtered and evaporated down using the rotary evaporator. The methyl 5-tert.-butyl-furan-2-carboxylate thus obtained is used further without any additional purification steps.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08865703B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-2db3cf5d459d43328f9035965ebf1810 |
| Source note | uspto-grants-2014_10 |