HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855231Generated: October 31, 2026
Triphenylphosphine → Methyl (R)-4-Chloro-3-hydroxybutyrate
https://huagongshe.com/reaction/1855231
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | methyl (3R)-3,4-dihydroxybutanoate | HCID 9877378 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl (R)-4-Chloro-3-hydroxybutyrate | HCID 10920707 | 26% |
Reaction Steps
To a solution of (R)-methyl 3,4-dihydroxybutanoate (125.1 g, 0.93 mol) in CH2Cl2 (1.8 L) was added PPh3 (244.5 g, 0.93 mol) and slowly added NCS (124.2 g, 0.93 mol) under ice water cooling. The mixture was stirred at 5° C. for 20 min and then stirred for 18 h at room temperature. After evaporating the solvent, the residue was purified by column chromatography (P.E\E.A 20:1-5:1, gradient) to give (R)-methyl 4-chloro-3-hydroxybutanoate (33 g, 26% over 3 steps). 1H NMR (300 MHz, CDCl3) δ 4.18-4.25 (m, 1H), 3.68 (s, 3H), 3.55-3.60 (m, 2H), 3.32-3.33 (d, J=4.2 Hz, 1H), 2.52-2.68 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962856B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-90a1c93a6b8e4932b8519de00d09528a |
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| Source note | uspto-grants-2015_02 |
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