HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533538Generated: October 26, 2026
Sodium Sulfite → Ethyl (2R)-4-{4'-[(di-tert-butoxyphosphoryl)oxy]biphenyl-4-yl}-2-methyl-2-(methylsulfonyl)butanoate
https://huagongshe.com/reaction/533538
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Di-tert-butyl N,N-Diisopropylphosphoramidite | HCID 853005 | — |
| Reactant | Ethyl (2R)-4-(4'-hydroxybiphenyl-4-yl)-2-methyl-2-(methylsulfonyl)butanoate | HCID 66579462 | — |
| Reactant | HCID 178418441 | HCID 178418441 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl (2R)-4-{4'-[(di-tert-butoxyphosphoryl)oxy]biphenyl-4-yl}-2-methyl-2-(methylsulfonyl)butanoate | HCID 66577870 | 91% |
Reaction Steps
A solution of 1H-tetrazole (2.37 g, 33.9 mmol, 3.0 equiv), di-tert-butyl-N,N-diisopropylphosphoramidite (7.42 mL, 22.6 mmol, 2.0 equiv), and ethyl(2R)-4-(4′-hydroxybiphenyl-4-yl)-2-methyl-2-(methylsulfonyl)butanoate (4.25 g, 11.3 mmol, 1.0 equiv) in tetrahydrofuran (113 mL) was allowed to stir overnight at room temperature. A solution of saturated sodium sulfite (330 mL) was added, and the mixture was extracted with dichloromethane (3×440 mL). The combined organic layers were washed with water (3×330 mL), brine (3×330 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica gel (50% ethyl acetate in heptane) to provide a colorless oil (5.84 g, 91%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.33 (t, J=7.13 Hz, 3H) 1.50-1.52 (m, 18H) 1.71 (s, 3H) 2.17-2.30 (m, 1H) 2.46-2.61 (m, 2H) 2.72-2.85 (m, 1H) 3.04 (s, 3H) 4.26 (qd, J=7.13, 1.27 Hz, 2H) 7.21-7.28 (m, 4H) 7.45-7.53 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853258B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-be947402c8f94724b7e6e7a24b3b420b |
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| Source note | uspto-grants-2014_10 |
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