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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435409Generated: October 28, 2026

Triethylamine → HCID 13071254, compound

https://huagongshe.com/reaction/435409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Methyleneisobenzofuran-1(3H)-oneHCID 10057627—
ReactantHCID 53983756HCID 53983756—
SolventDiethyl EtherHCID 3283—
ProductHCID 13071254HCID 1307125458.7%

Reaction Steps

To a solution of o-tolualdehyde chlorooxime (26.8 g, 0.158 mole), 3-methylenephthalide (14.6 g, 0.1 mole) and ether (400 ml.) was added dropwise a solution of triethylamine (16 g, 0.158 mole) in 30 ml. of ether at 5°-10° C. in 45 minutes. The mixture was stirred at room temperature for 40 hours and filtered. The solid material collected was dissolved in 1 liter of chloroform and 200 ml. of water. The chloroform solution was then washed two times with water, dried over CaSO4 and concentrated under vacuum to give 16.4 g of white solid, m.p. 146°-149° C. The original ether solution was washed two times with water, dried over CaSO4 and concentrated to 100 ml. Another 1.64 g of the spiro compound precipitated out. The ether solution was then further concentrated to 10.8 g of yellow-brown oil which did not contain a significant amount of the desired product. Recrystallization of 12 g of the crude spiro compound from tetrahydrofuran-ether gave 9.87 g of a pure white solid, m.p. 159°-164° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04401457
Source datasetuspto-grants-1983_08
ORD IDord-f75323e008914209a6f0a0c51d21d7dc
Source noteuspto-grants-1983_08