HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 6-Bromo-3,4-dihydro-2H-1-benzopyran-2-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | 6-Bromo-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid | HCID 22351390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Bromo-3,4-dihydro-2H-1-benzopyran-2-methanol | HCID 20211050 | 86% |
Reaction Steps
To a stirred mixture of 80 parts of 6-bromo-3,4-dihydro-2H-benzopyran-2-carboxylic acid and 225 parts of tetrahydrofuran were added dropwise 400 parts of a solution of borane, compound with thiobismethane 0.2N in tetrahydrofuran. Upon completion, stirring was continued for 4hours at room temperature. 80 parts of methanol were added dropwise and stirring was continued for 30 minutes at reflux temperature. The solvent was distilled off till half its volume. The remaining solvent was evaporated and the residue was distilled, yielding 63 parts (86%) of 6-bromo-3,4-dihydro-2H-1-benzopyran-2-methanol; bp. 150° C. at 39.9 Pa (intermediate 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04654362 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-00b34106b0ca4ad589a61fd6922c9c6a |
| Source note | uspto-grants-1987_03 |