HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20408Generated: October 26, 2026
Tetrabutylammonium Fluoride → HCID 68561911, compound
https://huagongshe.com/reaction/20408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 1,3-Difluoro-5-(2-nitroethyl)benzene | HCID 55250753 | — |
| Reactant | (2R,5R)-2-(2,2-Dimethylpropoxy)-5-formylmorpholine-4-carboxylic acid tert-butyl ester | HCID 86615359 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68561911 | HCID 68561911 | 34% |
Reaction Steps
Add tetrabutylammonium fluoride (18.32 mL, 18.32 mmol, 1.0 M in tetrahydrofuran) to (2R,5R)-2-(2,2-dimethylpropoxy)-5-formylmorpholine-4-carboxylic acid tert-butyl ester (5.02 g, 16.66 mmol) and 1,3-difluoro-5-(2-nitroethyl)-benzene (3.43 g, 18.32 mmol) in tetrahydrofuran (28 mL) at −10° C. and stir 20 minutes. Pour into ice cold saturated aqueous sodium chloride and extract with ethyl acetate. Wash with 0.1 N aqueous citric acid and saturated aqueous sodium chloride, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 20:80 to 30%:70 diethyl ether:hexanes) to give a mixture of 2 diastereomers (3.66 g, 75:25 mixture) which are separated using chiral chromatography to give the desired compound (˜2.45 g, 34.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745438B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-be30b5997f8b4be99dee6c5b4bacce7b |
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| Source note | uspto-grants-2010_06 |
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