HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727236Generated: October 30, 2026
Phenothiazine → 10-(3-chloropropyl)-10H-phenothiazine
https://huagongshe.com/reaction/727236
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 10-(3-chloropropyl)-10H-phenothiazine | HCID 12299120 | 80% |
Reaction Steps
To a solution of phenothiazine (4.0 g, 0.02 mol) in dry dimethylformamide (100 ml) kept under an atmosphere of nitrogen, sodium hydride (1.0 g, 0.025 mol, 60% dispersion in oil) was carefully added. The reaction mixture was left stirring for 15 minutes. 1-Bromo-3-chloropropane (8.0 g, 0.05 mol) was added and the mixture was left stirring overnight. Ammonium chloride (2.0 g, 0.04 mol) was added, and after continued stirring for 30 minutes the solution was poured onto water (300 ml). The mixture was extracted with dichloromethane (2×200 ml). The combined organic extracts were dried (MgSO4), filtered and the solvent evaporated. This afforded a residue which was purified by column chromatography on silica gel (250 g) using a mixture of n-heptane and ethyl acetate (9:1) as eluent. 4.4 g (80%) of 10-(3-chloropropyl)-10H-phenothiazine was obtained as an oil. Rf : 0.55 (SiO2 ; n-heptane/ethyl acetate=1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05712292 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-997ad8ed80e34f909dbd16f59fa4e8ca |
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| Source note | uspto-grants-1998_01 |
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