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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395181Generated: November 4, 2026

1-(Chloromethoxy)-2-methoxyethane → 10-Hexyl-3,7-dimethoxy-4-(2-methoxyethoxymethoxymethyl)-phenothiazine

https://huagongshe.com/reaction/2395181

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
ReactantLithium borohydrideHCID 4148881—
Reactant10-Hexyl-3,7-dimethoxyphenothiazine-4-methanolHCID 18972544—
Reactant10-Hexyl-3,7-dimethoxy-phenothiazine-4-carbaldehydeHCID 18972606—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventDiethylether hexaneHCID 21584099—
Product10-Hexyl-3,7-dimethoxy-4-(2-methoxyethoxymethoxymethyl)-phenothiazineHCID 18972547—

Reaction Steps

A solution of 2.39 g (6.43 mmol) of 10-hexyl-3,7-dimethoxy-phenothiazine-4-carbaldehyde in 30 ml of tetrahydrofuran was reduced with 7.0 ml of lithium borohydride solution (1M in tetrahydrofuran) analogously to that described in Example 4.1.1.da. The resulting 10-hexyl-3,7-dimethoxy-phenothiazine-4-methanol was reacted with 4.0 ml of n-butyllithium solution (1.6M in hexane) and 1.0 g (8.0 mmol) of 2-methoxyethoxymethyl chloride analogously to that described in Example 4.1.1.db. After chromatography on silica gel with diethyl ether/hexane (3:2) 2.33 g (78.5%) of 10-hexyl-3,7-dimethoxy-4-(2-methoxy-ethoxymethoxymethyl)-phenothiazine were obtained as a light yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811548
Source datasetuspto-grants-1998_09
ORD IDord-4ab05ff76a83408b9d85b88fb5bac813
Source noteuspto-grants-1998_09