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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764143Generated: November 3, 2026

Isopropylamine → HCID 53827166, compound

https://huagongshe.com/reaction/1764143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
ReactantTriethylamineHCID 8471—
ReactantHCID 54077320HCID 54077320—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53827166HCID 53827166—

Reaction Steps

To a solution of 5 g of isopropylamine and 5 ml of triethylamine in 100 ml of absolute tetrahydrofuran is slowly added dropwise with stirring at -5° C a solution of 13 g of α-[p-(1-cyclohexenyl)-phenoxy]-heptanoic acid chloride in 25 ml of absolute tetrahydrofuran. The reaction mixture is left to stand for 5 hours at room temperature, then evaporated in vacuo to dryness. The residue is partitioned between methylene chloride and 2N hydrochloric acid. The organic phase is washed with saturated sodium bicarbonate solution and water, dried over sodium sulphate and evaporated in vacuo. The residue yields the crude α-[p-(1-cyclohexenyl)-phenoxy]-heptanoic acid isopropylamide of the formula ##STR23## (m.p. 86°-88° C after recrystallisation from petroleum ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04115416
Source datasetuspto-grants-1978_09
ORD IDord-0ddebb94115046419fc6b3f78c445f31
Source noteuspto-grants-1978_09