HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017769Generated: October 30, 2026
Butanoic acid, 4-chloro-, methyl ester → HCID 22897426, compound
https://huagongshe.com/reaction/1017769
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butanoic acid, 4-chloro-, methyl ester | HCID 76612 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 22897431 | HCID 22897431 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22897426 | HCID 22897426 | — |
Reaction Steps
To a solution of 65 mg of 1-(S)-(1-(R)-(3,5-bis(trifluoromethyl)-phenyl)ethoxy)-2-(R)-(4-fluorophenyl)-3-(R)-((methylamino)methyl)cyclopentane from Example 18, Step B in 1 mL of acetonitrile was added 0.019 mL of methyl 4-chlorobutyrate and 0.037 mL of DIPEA. The reaction was heated at 50° C. for 48 hours, then an additional 0.038 mL of methyl 4-chlorobutyrate, 0.074 mL of DIPEA and 3 mg of tetrabutylammonium iodide were added and heating continued at 70° C. for 48 hours. The reaction was evaporated under a stream of nitrogen and the residue purified by prep TLC (10% methanol in ethyl acetate) to give 41 mg of title compound and 17 mg of recovered starting material. Mass spec (ESI): 564 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479518B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-409f641db2504f5cb93faa07bf3450bf |
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| Source note | uspto-grants-2002_11 |
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