HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703236Generated: October 29, 2026
Hydrochloric Acid → HCID 57235519, compound
https://huagongshe.com/reaction/703236
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 54396025 | HCID 54396025 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57235519 | HCID 57235519 | 70.4% |
Reaction Steps
To a solution of 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-3-[1-[[(tetrahydro-2H-pyran-2-yl)oxy]imino]ethyl]-1H-indole (5.0 g, 11.3 mmol) in tetrahydrofuran (115 ml) is added 10 ml of concentrated hydrochloric acid. The reaction mixture is stirred for 21/2 hours, at which time it is neutralized with concentrated ammonium hydroxide. It is concentrated to near dryness, diluted with ethyl acetate and washed twice with water and once with a saturated solution of sodium chloride. The organic phase is further dried over magnesium sulfate, filtered, and concentrated slowly in vacuo to 50 ml. The powdery crystals are collected to give 2.8 g (70.4%) of pure 1-(4-chlorobenzoyl)-3-[1-(hydroxyimino)ethyl]-5-methoxy-2-methyl-1H-indole; mp darkens (chars) at 170°-197° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04981865 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-6a2dfe87daf140ec93586932ee72040c |
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| Source note | uspto-grants-1991_01 |
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