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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381653Generated: October 27, 2026

Water → N-alpha-Phenylethylphenoxazine

https://huagongshe.com/reaction/1381653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(1-Chloroethyl)benzeneHCID 12648—
ReactantSodium hydrideHCID 24758—
ReactantPhenoxazineHCID 67278—
SolventDimethylformamideHCID 6228—
ProductN-alpha-PhenylethylphenoxazineHCID 14031257—

Reaction Steps

A solution of phenoxazine 76 g, 0.417 mol (Aldrich Chemical Co., Milwaukee, WI, Cat. No. P1,585-8) in dry dimethylformamide (120 ml) was added to a stirred suspension of sodium hydride (22 g, 0.458 mol, 50% suspension in mineral oil) in dry dimethylformamide (500 ml). After 1 hour at room temperature α-phenylethyl chloride (59 g, 0.43 mol) was added dropwise and when the addition was completed, stirring was continued for another 30 min. The solution was poured into water, the product extracted with ethyl acetate, the extract washed with water, and dried over sodium sulfate. The solvent was removed under reduced pressure. N-α-Phenylethylphenoxazine was crystallized from ether-hexane, mp 100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803269
Source datasetuspto-grants-1989_02
ORD IDord-ab7e71828ee44375a5c16f403db80541
Source noteuspto-grants-1989_02