HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424280Generated: November 1, 2026
Ethyl 4-iodobenzoate → Ethyl(+/-)-4-(4,4,4-trifluoro-1-hydroxybutyl)benzoate
https://huagongshe.com/reaction/1424280
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-iodobenzoate | HCID 142891 | — |
| Reactant | 4,4,4-Trifluorobutanal | HCID 2777083 | — |
| Reactant | HCID 178461733 | HCID 178461733 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl(+/-)-4-(4,4,4-trifluoro-1-hydroxybutyl)benzoate | HCID 68178660 | — |
Reaction Steps
To a solution of the ethyl 4-iodobenzoate (1.21 ml, 7.24 mmol) in tetrahydrofuran (12 ml) at −40° C. was added isopropylmagnesium chloride lithium chloride complex (6.13 ml, 7.97 mmol, 1.3 M in tetrahydrofuran) dropwise. The mixture was stirred for approximately 1 hour whereupon 4,4,4-trifluorobutanal (0.761 ml, 0.724 mmol) was added dropwise. The mixture was stirred at −40° C. for 15 minutes and slowly warmed to ambient temperature over 12 hours. The reaction was quenched with aqueous 1.0 M hydrochloric acid, and the aqueous layer was extracted with ethyl acetate (3×). The combined organic layers were dried over magnesium sulfate, filtered, and concentrated under reduced pressure to give ethyl(+/−)-4-(4,4,4-trifluoro-1-hydroxybutyl)benzoate, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927577B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-2984da2e703844dd9f8775ee277a6f8b |
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| Source note | uspto-grants-2015_01 |
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