HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenethylamine, (+)- → (R)-chroman-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenethylamine, (+)- | HCID 643189 | — |
| Reactant | 3,4-dihydro-2H-1-benzopyran-2-carboxylic acid | HCID 2723665 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-chroman-2-carboxylic acid | HCID 6933107 | 13.4% |
Reaction Steps
A solution of (+)-(R)-α-methylbenzylamine (0.37 mol) in ethanol (100 ml) was added to a solution of 3,4-dihydro-2H-1-benzopyran-2-carboxylic acid (0.36 mol) in ethanol (200 ml). The mixture was allowed to crystallize out. The precipitate was filtered off and dried. The residue was crystallized 4 times from ethanol. The precipitate was filtered off and dried. The residue was taken up in water, treated with HCl 10% and extracted with diethyl ether. The organic layer was separated, dried, filtered and the solvent was evaporated, yielding 8.6 g of (-)-(R)-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid (mp. 85.5° C., [α]20D =-6.7° (c=100 mg/10 ml in methanol)) (interm. 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06133277 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-ea3c0711151d422daadca0802694e12a |
| Source note | uspto-grants-2000_10 |