HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → HCID 54511739, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | PHENYLACETIC ACID,2-(2'-CL-6-ME)ANILINO | HCID 14762933 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54511739 | HCID 54511739 | — |
Reaction Steps
To a solution of 10 g of [o-(3-chloro-o-toluidino)-phenyl]-acetic acid (M.P. 124°-125°) in 100 ml of ether are slowly added dropwise 100 ml of 2% ethereal diazomethane solution. The solution is allowed to stand for 2 hours at room temperature, and then concentrated to dryness at 40° under 11 Torr. The residue is dissolved in 100 ml of ether. The ether solution is extracted with 40 ml of 2 N sodium hydrogen carbonate solution and water, dried over sodium sulphate, and concentrated at 40° under 11 Torr. The residue is crystallised from benzine. The obtained [o-(3-chloro-o-toluidino)-phenyl]-acetic acid methyl ester melts at 47°-48°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04173577 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-58be13430ee34970ae87133a81ac63ef |
| Source note | uspto-grants-1979_11 |