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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274062Generated: October 31, 2026

3-Nitro-6,7,8,9-tetrahydro-5H-benzo[a]cyclohepten-5-one → 3-nitro-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol

https://huagongshe.com/reaction/274062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitro-6,7,8,9-tetrahydro-5H-benzo[a]cyclohepten-5-oneHCID 344487—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product3-nitro-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-olHCID 2239180296.3%

Reaction Steps

To a suspension of 3-nitro-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-one (7.0 g) in methanol (70 ml), sodium borohydride (1.29 g) was added portionwise at 21°-30° C. and the whole was stirred for 1 hour. The solution was poured into ice water (210 ml) and the resulting precipitate was collected by filtration, washed with water and dried to give 3-nitro-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol (6.81 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387710
Source datasetuspto-grants-1995_02
ORD IDord-8725762c71a84aa793e45c0776afc080
Source noteuspto-grants-1995_02