HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (+/-)-6-Benzyloxy-2,5,7,8-tetramethylchroman2-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | (R)-6-benzyloxy-2,5,7,8-tetramethylchroman-2-acetic acid | HCID 54154878 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (+/-)-6-Benzyloxy-2,5,7,8-tetramethylchroman2-acetic acid | HCID 14368743 | — |
Reaction Steps
To a solution of 11.0 g. of diisopropylamine in 50 ml. of anhydrous tetrahydrofuran at 0° was added 50 ml. of 2N butyllithium solution. To the resultant solution of lithium diisopropylamide was added a solution of 3.54 g. of (R)-6-benzyloxy-2,5,7,8-tetramethylchroman-2-acetic acid in 25 ml. of tetrahydrofuran. The resulting mixture was heated at 50° for 4 hours, acidified with 2N HCl and extracted with ether. The ether solutions were washed with brine, dried (Na2SO4) and stripped of solvent to give (±)-6-benzyloxy-2,5,7,8-tetramethylchroman-2-acetic acid, [α]D25 =±0°, m.p. 130°-133° .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04018799 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-dafdd73d4aa8468cace542839fd7f0e5 |
| Source note | uspto-grants-1977_04 |