HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27946Generated: October 29, 2026
Water → 3-Benzylpyrrolylmethyl 2-(5-trifluoromethyl-2-benzothienyl)-3-methylbutanoate
https://huagongshe.com/reaction/27946
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(5-Trifluoromethyl-2-benzothienyl)-3-methylbutanoic acid | HCID 53945785 | — |
| Reactant | 3-Benzyl-1-pyrrolylmethanol | HCID 54343081 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-Benzylpyrrolylmethyl 2-(5-trifluoromethyl-2-benzothienyl)-3-methylbutanoate | HCID 54276535 | — |
Reaction Steps
A mixture of 2-(5-trifluoromethyl-2-benzothienyl)-3-methylbutanoic acid (3.95 mmol), thionyl chloride (0.342 ml, 4.74 mmol) and DMF (several drops) in 50 ml benzene is stirred at RT for 2 days. The solvent and excess thionyl chloride are evaporated under reduced pressure. The resulting acid chloride is dissolved in 50 ml benzene, and 3-benzylpyrrolylmethyl alcohol (3.95 mmol) and 0.482 g 4-dimethylaminopyridine (3.95 mmol) are added. The mixture is left at 25° for 18 hours and then heated under reflux for 2 hours. The mixture is then poured into water and extracted with ether. The organic phase is washed with dilute HCL, sat. NaHCO3, water and brine, dried and solvent removed under vacuum to yield 3-benzylpyrrolylmethyl 2-(5-trifluoromethyl-2-benzothienyl)-3-methylbutanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04224330 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-c40e7b1588574efd95d601e70ef488b0 |
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| Source note | uspto-grants-1980_09 |
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