HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzoyl chloride → HCID 131711131, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | HCID 12878609 | HCID 12878609 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 131711131 | HCID 131711131 | — |
Reaction Steps
Ten grams of 2-[[[2-[3-(Dimethylamino)propoxy]-phenyl]methyl]amino]acetamide (see Example 2B) and 7.1 g of p-chlorobenzoyl chloride are reacted in 110 ml of chloroform as described in Example 1. The finely-divided, solid product separates at the end of the addition; crude yield, after standing for about 16 hours at room temperature, 10.2 g; melting point 195°-197° C dec, sintering at 175° C. Work-up of the mother liquor does not yield any additional product. Following crystallization (of 9.7 g) from 50 ml of warm methanol - 100 ml of ether, the material weighs 6.3 g; melting point 198°-200° C, dec, sintering at 175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04098789 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-930b9b0c391e4bd68c18b59e2af6b747 |
| Source note | uspto-grants-1978_07 |