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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226738Generated: November 1, 2026

Water → HCID 18965314, compound

https://huagongshe.com/reaction/2226738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenothiazineHCID 7108—
ReactantSodium hydrideHCID 24758—
Reactant2-[2-(2-Chloroethoxy)ethoxy]oxaneHCID 10965737—
SolventDichloromethaneHCID 6344—
SolventButyl etherHCID 8909—
ProductHCID 18965314HCID 1896531455.3%

Reaction Conditions

Temperature135 °C

Reaction Steps

Phenothiazine (3.8 g, 19 mmol) was added to a suspension of sodium hydride (0.92 g, 23 mmol, 60% oil dispersion) in dry dibutylether (25 ml) under an atmosphere of nitrogen. The mixture was heated at 135° C. for 1 h and then cooled to approximately 100° C. 2-(2-((tetrahydro-2-pyranyl)oxy)ethoxy)ethylchloride (8 g, 38 mmol) was added in one portion and the mixture was heated overnight at 110° C. The reaction mixture was poured into water (250 ml) and extracted with dichloromethane (3×50 ml) and diethyl ether (50 ml). The combined organic extracts were washed with brine and dried over sodium sulphate. The solvent was evaporated in vacuo leaving an oil, which was submitted to column chromatography using dichloromethane as eluent. Collecting the proper fractions afforded 3.9 g of crude 10-(2-(2-((tetrahydro-2-pyranyl)oxy)ethoxy)ethyl)-10H-phenothiazine. TLC: rf=0.72 (SiO2 ; dichloromethane/methanol=19:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348965
Source datasetuspto-grants-1994_09
ORD IDord-d6041f89af2f4048ba1c3adb14d74cf5
Source noteuspto-grants-1994_09