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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400045Generated: November 1, 2026

Hydrochloric Acid → HCID 19382375, compound

https://huagongshe.com/reaction/2400045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Furoic acidHCID 10268—
ReactantLithium diisopropylamideHCID 2724682—
ReactantN-Methoxy-N-methylpivalamideHCID 11446410—
ReactantTetrahydrofuran heptane ethylbenzolHCID 22742125—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19382375HCID 1938237562.4%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of 3-furoic acid (8.97 g, 0.08 mol) in tetrahydrofuran (200 ml) was cooled to -70° C. and a 2.0M solution of lithium diisopropylamide in THF-ethylbenzene-heptane (80 ml, 0.16 mol) was added dropwise over 3/4 hr at -70° to -20° C. under nitrogen to give a tan suspension. A red solution formed after stirring for 113/4 hours at -20° C. To this solution was added N-methoxy-N-methylpivalamide (11.67 g, 0.08 mol) in tetrahydrofuran (10 ml) at -40° C. The reaction mixture was left at ambient temperature overnight. Then ,it was cooled in ice and neutralized with 6N ethanolic hydrogen chloride (50 ml). The neutralized solution was acidified with 1.5N HCl (150 ml) and was extracted with ether (300 ml). The ether extracts were washed with saturated NaCl, dried over Na2SO4, filtered and concentrated in vacuo to a brown solid (15.4 g). Chromatography on silica gel using hexane-THF-acetic acid (10-2-0.2) gave a yellow solid (9.8 g), mp 85°-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05453424
Source datasetuspto-grants-1995_09
ORD IDord-f60236869e37428fb6d6cd8b4467a2da
Source noteuspto-grants-1995_09