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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615929Generated: October 30, 2026

Tetrahydrofuran → HCID 15592210, compound

https://huagongshe.com/reaction/615929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 15592209HCID 15592209—
ReactantButyllithiumHCID 178418339—
ProductHCID 15592210HCID 15592210—

Reaction Steps

A solution of the product of Example 4 (4 mmoles) in tetrahydrofuran (150 ml) was cooled to ca.-75° C. under an atmosphere of argon. n-Butyllithium (2 ml, 2.04 M in hexane) was added by syringe over 15 min. while maintaining the reaction temperature below -70° C., and the solution then stirred for 3.5 hours. A cold solution (ca.-8° C.) of octadecyl aldehyde (4 mmoles) in tetrahydrofuran (100 ml) was canulated by syringe to the above solution over 25 min., keeping the temperature below -60° C. The reaction temperature rose to 25° C. during the next 2 hours, after which the reaction was quenched with water (10 ml) and stirred overnight. After removing the tetrahydrofuran under a nitrogen stream, water (75 ml) was added and the product extracted into ethyl acetate. The combined extract was dried over sodium sulfate, filtered and stripped under reduced pressure to give 1.7 g of an oil. The product was purified by chromatography on silica gel to give 0.85 g of the title compound, m.p. ca.74°-78° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04501895
Source datasetuspto-grants-1985_02
ORD IDord-69916678aca64d2a97666ee06b86e3dc
Source noteuspto-grants-1985_02