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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417332Generated: November 2, 2026

Dimethylformamide → 6-Bromo-1,2,3,4-tetrahydro-7-methoxy-1,1,4,4-tetramethylnaphthalene

https://huagongshe.com/reaction/2417332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant3-Bromo-2-hydroxy-5,6,7,8-tetrahydro-5,5,8,6-tetramethylnaphthaleneHCID 22634661—
SolventWaterHCID 962—
Product6-Bromo-1,2,3,4-tetrahydro-7-methoxy-1,1,4,4-tetramethylnaphthaleneHCID 10732746—

Reaction Steps

7 g (24.7 mmol) of 3-bromo-2-hydroxy-5,6,7,8-tetrahydro-5,5,8,6-tetramethylnaphthalene and 40 ml of DMF are introduced into a three-necked flask under a stream of nitrogren. 890mg (29.6 mmol) of sodium hydride (80% in oil) are added portionwise and the mixture is stirred until the evolution of gas has ceased. 1.7 ml (27 mmol) of iodomethane are then added and the mixture is stirred at room temperature for one hour. The reaction medium is poured into water and extracted with ethyl ether, and the organic phase is separated out after settling has taken place, dried over magnesium sulphate and evaporated. 7.3 g (99%) of the expected product are collected in the for of an oil which crystallizes slowly. Melting point 77-8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825360B1
Source datasetuspto-grants-2004_11
ORD IDord-008e8bcc101a4b898d82a80b1c110083
Source noteuspto-grants-2004_11