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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367276Generated: October 28, 2026

Acetone → (2R)-3,4-Dihydro-2H-1-benzopyran-2-methanol

https://huagongshe.com/reaction/367276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantTolueneHCID 1140—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
Product(2R)-3,4-Dihydro-2H-1-benzopyran-2-methanolHCID 7170029—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of toluene (1000 ml) and ethanol (absolute, 520 ml) was stirred. Sodium borohydride (2.13 mol) was added at room temperature, under an inert atmosphere. The mixture was heated to 50° C. Intermediate (2) (2.14 mol) was added dropwise at 50° C. in a 90-minutes period (exothermic temperature rise of 15° C.; cooling required). The reaction mixture was stirred for 90 minutes at 50° C. Water (1500 ml) was added while stirring. Then, 2-propanone (100 ml) was added dropwise under slight cooling. The mixture was decomposed with HCl (180 ml). The organic layer was separated, dried, filtered and the solvent evaporated, yielding 295 g of (-)-(R)-3,4-dihydro-2H-1-benzopyran-2-methanol (interm. 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133277
Source datasetuspto-grants-2000_10
ORD IDord-ae668af34f7245bf9cf7d74adb418c83
Source noteuspto-grants-2000_10