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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361002Generated: October 26, 2026

Sodium hydride → 8-(6-Formylnaphthalen-2-yloxy)octanoic acid

https://huagongshe.com/reaction/1361002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant8-Bromooctanoic acidHCID 548275—
Reactant6-Hydroxy-2-naphthaldehydeHCID 2764110—
ReactantSodiumHCID 5360545—
ReactantNaphtholateHCID 12168161—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
Product8-(6-Formylnaphthalen-2-yloxy)octanoic acidHCID 5745703956.1%

Reaction Steps

The intermediate aldehyde for this compound was prepared by a slightly modified procedure: 6-Hydroxynaphthalene-2-carbaldehyde (1.0 g, 5.8 mmol) was dissolved in DMF (10 mL) and sodium hydride 60% (278 mg) was added and the mixture stirred at RT for 15 min. 8-Bromooctanoic acid (0.37 g, 1.7 mmol) was converted to the sodium salt by addition of sodium hydride 60% and added to an aliquot (2.5 mL) of the above naphtholate solution and the resulting mixture was stirred at RT for 16 hours. Aqueous acetic acid (10%) was added and the mixture was extracted 3 times with diethyl ether. The combined organic phases were dried with MgSO4 and evaporated to dryness affording 300 mg of 8-(6-formylnaphthalen-2-yloxy)octanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879893B2
Source datasetuspto-grants-2011_02
ORD IDord-7160a50037724d7182b890bf5e632b28
Source noteuspto-grants-2011_02