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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041840Generated: October 31, 2026

Phosphorus oxychloride → HCID 67114181, compound

https://huagongshe.com/reaction/1041840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant144537-21-3HCID 67114267—
ProductHCID 67114181HCID 67114181112.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557738B2
Source datasetuspto-grants-2013_10
ORD IDord-e16e9c33ce41492db6a57371c543d05a
Source noteuspto-grants-2013_10