Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175704Generated: October 29, 2026

3,4-Dihydro-6,7-dimethoxy-1(2H)-naphthalenone → 6,7-Dimethoxy-1,2,3,4-tetrahydronaphthalen-1-ol

https://huagongshe.com/reaction/2175704

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dihydro-6,7-dimethoxy-1(2H)-naphthalenoneHCID 266816—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product6,7-Dimethoxy-1,2,3,4-tetrahydronaphthalen-1-olHCID 6273545593%

Reaction Steps

To a stirred solution of 6,7-dimethoxy-3,4-dihydronaphthalen-1(2H)-one (3.09 g, mmol) in MeOH (50 mL) was added NaBH4 (680 mg, 18 mmol) portion wise over 0.5 hour. The resulting mixture was stirred at room temperature overnight. The reaction was quenched with 1N HCl, diluted with water and extracted with DCM. The combined organic phase was washed with brine, dried over sodium sulfate and the solvent was removed under reduced pressure to afford 6,7-dimethoxy-1,2,3,4-tetrahydronaphthalen-1-ol as a yellow oil (2.9 g, 93%). LC-MS (ES-API); rt 7.96 min; m/z calculated for C12H16O3 [M+Na]+ 231.1, found 231.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062076B2
Source datasetuspto-grants-2015_06
ORD IDord-329be3ed71694273b60b9bf989828d65
Source noteuspto-grants-2015_06