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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258629Generated: October 30, 2026

Tetrahydrofuran → HCID 131710833, compound

https://huagongshe.com/reaction/258629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPivalolactoneHCID 16059—
ProductHCID 131710833HCID 131710833—

Reaction Steps

After 0.5 hour at 60° C., the solution was cooled to room temperature and 5.5 ml of pivalolactone was added. The resultant mixture was warmed slightly, and in about 15 minutes gelation occurred and it became too viscous to stir. It was let stand at room temperature overnight, and then was mixed with 250 ml of tetrahydrofuran. The mixture was transferred to a blender, and after being blended it was centrifuged. Extraction with THF showed no homopolyisoprene. The mixture was finally processed in a blender with about an equal volume of ethanol containing acetic acid and phenyl-β-naphthylamine antioxidant. The shredded polymer was separated on a filter and dried at room temperature under vacuum; yield, 12.5 g (80%, based on starting materials). Analysis by I. R. indicated approximately 45% pivalolactone in the polymer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04034021
Source datasetuspto-grants-1977_07
ORD IDord-1be9a718ad7e4de8a7affe793a96f9d5
Source noteuspto-grants-1977_07