HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428366Generated: October 25, 2026
Potassium Hydroxide → 3-(Methylsulfanyl)pentanoic acid
https://huagongshe.com/reaction/1428366
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | S,S-dimethyl carbonodithioate | HCID 313474 | — |
| Reactant | trans-2-Pentenoic acid | HCID 638122 | — |
| Product | 3-(Methylsulfanyl)pentanoic acid | HCID 57274283 | 151.8% |
Reaction Steps
S,S-dimethyl carbonodithioate (1.467 g, 12.00 mmol) was added with vigorous stirring to a solution of (E)-pent-2-enoic acid (2.002 g, 20 mmol) in 30% KOH solution (prepared from potassium hydroxide (3.87 g, 69 mmol) and Water (10 mL)). The reaction mixture was slowly heated to 90° C. over a period of 20-30 min Heating was continued for 3 hours before the reaction was cooled down to 25° C. and quenched slowly with HCl. The mixture was then extracted with DCM (3×30 mL), combined organic layer dried and concentrated to give 3-(methylthio)pentanoic acid (2.7 g, 18.22 mmol, 91% yield) as light orange oil: IR (Thin film) 2975, 1701 cm−1; 1H NMR (400 MHz, CDCl3) δ 2.92 (qd, J=7.3, 5.6 Hz, 1H), 2.63 (d, J=7.2 Hz, 2H), 2.08 (s, 3H), 1.75-1.51 (m, 2H), 1.03 (t, J=7.4 Hz, 3H); 13C NMR (101 MHz, CDCl3) δ 178.14, 43.95, 39.78, 27.04, 12.95, 11.29; EIMS m/z 148.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937083B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-bd5cb13c32ca443ea99e48016fa60c92 |
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| Source note | uspto-grants-2015_01 |
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