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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-carbaldehydeHCID 2795471—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product(2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-yl)methanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04748186
Source datasetuspto-grants-1988_05
ORD IDord-ae76aa1618574f12b160277ac1b3ac6d
Source noteuspto-grants-1988_05