HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231046Generated: October 27, 2026
Methyl chloroformate → 4-chloro-3-isobutyryloxy-10H-phenothiazine
https://huagongshe.com/reaction/231046
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Isobutyric Acid | HCID 6590 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-chloro-3-hydroxy-10H-phenothiazine | HCID 9881418 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-chloro-3-isobutyryloxy-10H-phenothiazine | HCID 13882030 | — |
Reaction Steps
To a solution of iso-butyric acid (1.6 ml) in THF (10 ml) at 0° C. was added Et3N (2.7 ml) and methylchloroformate (1.5 ml). To this resulting suspension was added slowly at 0° C. a solution of 4-chloro-3-hydroxy-10H-phenothiazine in THF (10 ml). The reaction mixture was stirred at 5° C. for 12 hours, after which H2O was added and the resulting aqueous phase extracted with ethyl acetate. The organic layer was then dried and evaporated. The resulting residue was purified by chromatography on silica gel to give 2.25 g of 4-chloro-3-isobutyryloxy-10H-phenothiazine (m.p. 155° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04845083 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-4eee8099bf5e42adb2288e40d48a137f |
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| Source note | uspto-grants-1989_07 |
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