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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472787Generated: October 26, 2026

Methyl 6-formyl-1-naphthoate → HCID 66660719, compound

https://huagongshe.com/reaction/472787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 6-formyl-1-naphthoateHCID 58056979—
ReactantHCID 178445865HCID 178445865—
SolventDiethyl EtherHCID 3283—
ProductHCID 66660719HCID 6666071971%

Reaction Steps

A solution of methyl 6-formyl-1-naphthoate (36 mg, 0.17 mmol) in THE (1.7 mL) was cooled to 0° C. and treated with n-pentylmagnesium bromide (0.1 mL of a 2.0 M solution in Et2O, 0.2 mmol). The cooling bath was removed and after stirring at room temperature for 1 h the reaction was quenched with 1 N aqueous HCl, diluted with water (10 mL) and extracted with EtOAc (3×10 The combined organic phase was dried (Na2SO4), filtered and concentrated in vacuo. The resulting residue was purified on 12 g silica gel (100% hexanes→40% EtOAc/hexanes, gradient) to afford 34 mg (71%) of methyl 6-(1-hydroxyhexyl)-1-naphthoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633220B2
Source datasetuspto-grants-2014_01
ORD IDord-419b4ccd0db946f99227bb7681fe07a1
Source noteuspto-grants-2014_01