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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236166Generated: October 28, 2026

Toluene → HCID 13726444, compound

https://huagongshe.com/reaction/236166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantHCID 13726439HCID 13726439—
SolventAcetonitrileHCID 6342—
ProductHCID 13726444HCID 13726444—

Reaction Steps

To a suspension of 9 g (0.02 mole) of phosphorus pentasulfide in 75 ml of acetonitrile was added 18 g (0.075 mole) of (R)-2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f]-1,4-oxazepine-5(4H)-one and the mixture was stirred at reflux for 2.5 hr, cooled and treated with 60 ml of toluene. The mixture was filtered and the solid washed twice with 30 ml of 25% acetonitrile-75% toluene. The volume was made to about 400 ml with 50% toluene-50% acetonitrile and extracted with saturated aqueous potassium bicarbonate. The organic layer was separated, treated with magnesium sulfate and charcoal, and filtered. The filtrate was concentrated and the residue was recrystallized from isopropyl alcohol-chloroform. Yield of title compound was 13 g (68%), m.p. 168°-170° C.; [α]D25 =(-) 47.4 (chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04642343
Source datasetuspto-grants-1987_02
ORD IDord-8f9ec6a5a4604925ae33ee86fb19cf05
Source noteuspto-grants-1987_02