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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4444Generated: October 25, 2026

Acetic Acid → 3-Hydroxymethyl-5-dichloromethyl-2-phthalimidopyrazine

https://huagongshe.com/reaction/4444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDichloromethaneHCID 6344—
ReactantPotassium AcetateHCID 517044—
Reactant3-Chloromethyl-5-dichloromethyl-2-phthalimidopyrazineHCID 13604769—
Solvent(Methanesulfinyl)methane--water (1/1)HCID 23503278—
Product3-Hydroxymethyl-5-dichloromethyl-2-phthalimidopyrazineHCID 1360477747%

Reaction Steps

50 ml of glacial acetic acid and 35 g of potassium acetate were added to a solution of 57.7 g (0.16 mole) of 65% strength 3-chloromethyl-5-dichloromethyl-2-phthalimidopyrazine in 1,000 ml of a 95:5 dimethyl sulfoxide/water mixture. The mixture was stirred for three days at room temperature, after which 1,000 ml of dichloromethane and 1,000 ml of ice-water were added, the resulting mixture was mixed thoroughly and phase separation was effected. The aqueous phase was washed once with 500 ml of dichloromethane and once with 250 ml of dichloromethane, and the combined organic phases were washed twice with 1,000 ml of water, dried over sodium sulfate and evaporated down. The resulting black oil was brought to crystallization with 50 ml of methanol, and then recrystallized from 700 ml of methanol. 16.6 g (47%) of 5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine of melting point 191°-192° C. (sublimation with decomposition) were obtained. 1H-NMR (200 MHz, CDCl3): δ3.3 (t, OH), 4.8 (d, 2H), 6.9 (s, 1H), 8.0 (m, 4H), 9.1 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04725689
Source datasetuspto-grants-1988_02
ORD IDord-e68e567d6ece4a128886cf5a849df771
Source noteuspto-grants-1988_02