Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | HCID 15000978 | HCID 15000978 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | HCID 72700536 | HCID 72700536 | 159.3% |
Reaction Steps
(S)-2-((tert-butoxycarbonyl)amino)-4-mercaptobutanoic acid (Boc-L-Hcs-OH) (188 mg, 0.4 mmol) was dissolved in H2O/THF (50% v/v, 16 mL). To the solution was added sodium thiomethoxide (560 mg, 8.0 mmol) at 0° C. Then, a solution of iodine in 95% EtOH was added dropwise until the color of the reaction system changed from colorless to brown. The mixture was stirred for 1.5 h with warming to room temperature. After removing THF under reduced pressure, reaction mixture was neutralized by 1 N HCl aq. until pH 2-3. The solution was extracted with EtOAc. The extract was washed with saturated NaS2O4 aq. and brine, and dried over MgSO4. Concentration under reduced pressure followed by flash chromatography over silica gel with EtOAc/Hexanes/AcOH (75:25:1) gave Boc-L-Hcm-OH (179.3 mg, 80% yield): 1H NMR (360 MHz, CDCl3) δ 5.06 (s, 1H), 4.44 (s, 1H), 2.78 (t, J=7.7 Hz, 2H), 2.42 (s, 3H), 2.35 (m, 1H), 2.09 (m, 1H), 1.45 (s, 9H); LRMS (ESI) m/z calcd for C10H20NO4S2 (M+H)+ 282.1. found 282.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376700B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-6151950de3c44caa894de9c4494b079d |
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| Source note | uspto-grants-2016_06 |
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