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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485725Generated: October 31, 2026

2H-chromen-6-ol → 3,4-Dihydro-2H-1-benzopyran-6-ol

https://huagongshe.com/reaction/485725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2H-chromen-6-olHCID 13437678—
CatalystChlorotris(triphenylphosphine)rhodium(I)HCID 84599—
SolventBenzeneHCID 241—
Product3,4-Dihydro-2H-1-benzopyran-6-olHCID 1512233893%

Reaction Steps

The 6-hydroxybenzopyran (1.5 g; 10 mM) was dissolved in 100 ml of anhydrous benzene along with Wilkinson's catalyst (280 mgs; 0.30 mM). This hydrogenation bottle containing this reaction mixture was first flushed with nitrogen and then with hydrogen. The bottle was pressurized to 40 psi in a Paar shaker and agitated for 40 minutes at which time the pressure in the bottle (400 ml dead volume) had droped to 30 psi and was dropping no further. The bottle was then flushed with nitrogen and the solvent was removed in vacuo. The residue was taken up in ether and filtered through a pad of celite. The solvent was removed and the oil was purified by flash chromatography on a 30 mm×6" column of silica gel eluted with 600 ml of 20% ethyl acetate in hexane. This purification produced 1.40 g (93%) of 2,3-dihydro-6-hydroxybenzopyran as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04537903
Source datasetuspto-grants-1985_08
ORD IDord-60df4bc6d0a24a39aa5a72f3c97daa18
Source noteuspto-grants-1985_08