HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263683Generated: November 1, 2026
Phosphorus oxychloride → HCID 59594371, compound
https://huagongshe.com/reaction/2263683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 59594400 | HCID 59594400 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59594371 | HCID 59594371 | 120% |
Reaction Steps
In a 1 L 3 neck RBF equipped with magnetic stir bar, condenser and N2 inlet, 7-chloro-1-(4-methoxybenzyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione (45 g, 0.136 mol) was suspended in 400 mL of toluene. To this was added N,N-dimethylanaline (33 g, 0.272 mol) followed by the addition of POCl3 (23 g) and the reaction stirred for 3 min (RT). Reaction flask was placed into a 90° C. oil bath and the reaction mixture was heated for 5 h and then cooled. The reaction was quenched by adding 450 mL of ice water and stirred for 15 min. The organic layer was separated and quickly washed with cold water (2×250 mL) and brine (300 mL). Then, the organic layer was dried over MgSO4, filtered and concentrated on a rotary evaporator to give 57 g of black crude product. Crude product was used for next step with no further purification. Yield 87.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07851465B2 |
|---|
| Source dataset | uspto-grants-2010_12 |
|---|
| ORD ID | ord-70573963eb4a4f13a22434a0a2bc3da7 |
|---|
| Source note | uspto-grants-2010_12 |
|---|