HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858955Generated: November 4, 2026
4-Fluorobenzenesulfonyl chloride → (R)-2-(4-fluoro-benzenesulfonylamino)-4-methyl-pentanoic acid
https://huagongshe.com/reaction/1858955
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | D-Leucine | HCID 439524 | — |
| Solvent | Water | HCID 962 | — |
| Product | (R)-2-(4-fluoro-benzenesulfonylamino)-4-methyl-pentanoic acid | HCID 6933578 | — |
Reaction Steps
A mixture of 4-fluoro-benzenesulfonyl chloride (1.65 g, 0.00848 mol), (R)-2-amino-4-methyl-pentanoic acid (1.233 g, 0.009398 mol), and sodium carbonate (1.91 g, 0.0180 mol) in water (15 mL) was stirred at room temperature for 5 days. The solution was filtered, and the filtrate was acidified with concentrated hydrochloric acid to pH=4. The mixture was extracted with ethyl acetate. The extract was washed with saturated sodium chloride, dried (MgSO4), and rotary evaporated to a yellow oil. The oil was chromatographed on silica gel (320 g, 230-400 mesh) eluting with dichloromethane-methanol (10:1, 10×300 mL). Fractions containing product were combined and rotary evaporated to give a pale yellow oil. The oil was dried in vacuo; yield 1.44 g (59%). 1H-NMR (DMSO-d6): δ8.1 (br s, 1H), 7.80 (m, 2H), 7.38 (m, 2H), 3.55 (t, 1H), 3.33 (br s, H2O),1.56 (m, 1H), 1.36 (dd, 2H), 0.75 (dd, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06153612 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-32c6118ccbbc4dca9021fa4145cc2b3c |
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| Source note | uspto-grants-2000_11 |
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