HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253229Generated: October 26, 2026
2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-carbaldehyde → (2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-yl)methanol
https://huagongshe.com/reaction/1253229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-carbaldehyde | HCID 2795471 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-yl)methanol | HCID 2795472 | — |
Reaction Steps
Sodium borohydride (1.08 grams, 0.0285 mole) was added carefully in small portions to a stirred solution of 2,3-dihydro-2,2-dimethylbenzofuran-7-carboxaldehyde (10.0 grams, 0.057 mole) in ethanol (150 ml) at 5°-10° C. during a ten minute period. The reaction mixture was stirred for thirty minutes and was then quenched by the dropwise addition of water (25 ml) followed by 10% hydrochloric acid (25 ml). The reaction mixture was concentrated under reduced pressure leaving a residue. This residue was partitioned between diethyl ether (75 ml) and 10% hydrochloric acid (30 ml). The layers were separated, and the organic layer was washed with water (40 ml) and a saturated aqueous solution of sodium chloride (40 ml). The dried (sodium sulfate) organic solution was concentrated under reduced pressure, yielding 2,3-dihydro-2,2-dimethylbenzofuran-7-ylmethanol as a solid. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04748186 |
|---|
| Source dataset | uspto-grants-1988_05 |
|---|
| ORD ID | ord-ae76aa1618574f12b160277ac1b3ac6d |
|---|
| Source note | uspto-grants-1988_05 |
|---|