HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041840Generated: October 31, 2026
Phosphorus oxychloride → HCID 67114181, compound
https://huagongshe.com/reaction/1041840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 144537-21-3 | HCID 67114267 | — |
| Product | HCID 67114181 | HCID 67114181 | 112.8% |
Reaction Steps
After adding phosphorous oxychloride (5 mL) and phosphorous pentachloride (0.65 g, 3.13 mmol) to 2,2-dimethyl-3,4-dihydro-2H-benzo[f][1,4]oxazepin-5-one (0.60 g, 3.13 mmol) (refer to the aforementioned Non-Patent Document 3 for a description of the synthesis method) at room temperature, the mixture was refluxed while heating for 5.5 hours. After allowing to cool to room temperature, the mixture was concentrated under reduced pressure and the residue was poured over crushed ice. The aqueous layer was extracted with ethyl acetate (50 mL) and the combined organic layer was washed twice with “saturated aqueous sodium bicarbonate solution (30 mL)+H2O (20 mL) and then with brine (30 mL) followed by drying with magnesium sulfate. After filtering, the solvent was distilled off under reduced pressure to obtain 0.74 g of 5-chloro-2,2-dimethyl-2,3-dihydro-benzo[f][1,4]oxazepine in the form of a brown oily substance. This substance was used in the next reaction without purifying further.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557738B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-e16e9c33ce41492db6a57371c543d05a |
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| Source note | uspto-grants-2013_10 |
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