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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382390Generated: November 2, 2026

Acetaminophen → HCID 13120352, compound

https://huagongshe.com/reaction/1382390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaminophenHCID 1983—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-Dichloro-2-butanolHCID 17021—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 13120352HCID 1312035253.5%

Reaction Steps

To a solution of 500 g (3.5 mole) of 1,4-dichloro-2-butanol was added, dropwise, 500 ml (6.25 mole) of a 50% sodium hydroxide solution. The mixture was stirred for 16 hr and then 500 ml of water was added, dropwise, with the temperature maintained below 35° C. The mixture was extracted with 500 ml of isopropyl ether, dried over sodium sulfate and concentrated to give an oil which was purified by distillation. To 14.3 g (0.1 mole) of the purified epoxide was added a solution of 15.1 g (0.1 mole) of 4-acetamidophenol in 150 ml of 2-propanol and 4 g of (0.1 mole) of sodium hydroxide in 10.0 ml of water. The mixture was stirred for 15 hr and then poured into 400 ml of water at 0° C. The crude, collected solid was washed with water and allowed to air dry. The solid was suspended in 350 ml of acetone, collected by filtration, and washed with additional portions of acetone. The filtrate was concentrated under reduced pressure to give 13.8 g (53% yield) of solid. A portion of this solid was recrystallized from tetrahydrofuran to give cream-colored solid, m.p. 124°-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04806555
Source datasetuspto-grants-1989_02
ORD IDord-bffb1100a8934613a85071a3d225f065
Source noteuspto-grants-1989_02