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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274080Generated: October 30, 2026

Sodium borohydride → 3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-ol

https://huagongshe.com/reaction/274080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Methoxy-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-oneHCID 10559574—
SolventMethanolHCID 887—
Product3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-olHCID 20094720—

Reaction Steps

To a solution of 3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-one (220 g) in methanol (1300 ml) was added portionwise sodium borohydride (22.0 g) at 6° C.-30° C., and then the reaction mixture was stirred for 40 minutes and evaporated in vacuo. The residue was partitioned between ethyl acetate (1 l) and water (1 l). The organic layer was washed with 1N hydrochloric acid (500 ml), aqueous sodium hydrogen carbonate (500 ml), and brine (200 ml), and dried over magnesium sulfate. The solvent was evaporated in vacuo to give 3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-ol as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387710
Source datasetuspto-grants-1995_02
ORD IDord-0361da08f81c4e1da779d4da0c028911
Source noteuspto-grants-1995_02