HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 23335145, compound → 3-Benzylpyrrolylmethyl 2-(6-chloro-2-benzothienyl)-3-methylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 23335145 | HCID 23335145 | — |
| Reactant | 2-(6-Chloro-2-benzothienyl)-3-methylbutanoic acid | HCID 54483118 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | 3-Benzylpyrrolylmethyl 2-(6-chloro-2-benzothienyl)-3-methylbutanoate | HCID 53837954 | — |
Reaction Steps
2-(6-Chloro-2-benzothienyl)-3-methylbutanoic acid (3.40 mmol) is stirred together with 0.34 g (3.40 mmol) KHCO3 in 10 ml THF/DMF (1:1) for 15 minutes. Then 3.40 mmol of 3-benzylpyrrolylmethyl methanesulfonate in 5 ml THF/DMF (1:1) is added and the mixture stirred for approximately 48 hours. The reaction is diluted with ether, washed with water (3×) and sat. NaCl, dried and solvent is removed to yield 3-benzylpyrrolylmethyl 2-(6-chloro-2-benzothienyl)-3-methylbutanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04224330 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-da9b10f718494464b4a8070d2fda862c |
| Source note | uspto-grants-1980_09 |