HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219791Generated: October 26, 2026
Acetic Acid → 3-Mercapto-2-(4-methoxy-benzylamino)-propionic acid
https://huagongshe.com/reaction/2219791
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(4-Methoxy-phenyl)-thiazolidine-4-carboxylic acid | HCID 2827728 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | 3-Mercapto-2-(4-methoxy-benzylamino)-propionic acid | HCID 11021047 | 68.1% |
Reaction Steps
A 22 L three-necked round bottom flask fitted with an internal temperature probe and a mechanical stirrer was charged with sodium borohydride (221.3 g, 5.85 mol). A 1.75 L portion of 0.25 M sodium hydroxide was added and the mixture was stirred until homogeneous. The solution was cooled to 0-5° C. 2-(4-methoxyphenyl)-thiazolidine-4-carboxylic acid (350.0 g, 1.46 mol) was dissolved in 2.1 L of a 0.62 M K2CO3 aqueous solution. The resulting solution was added to the solution of sodium borohydride while maintaining an internal temperature of below 30° C. The reaction was stirred until HPLC analysis showed no remaining starting material (approximately 1 hour). The reaction was cooled to 0° C. and 700 mL of glacial acetic acid was added with stirring. The final pH of the reaction mixture was approximately 5. The resulting white solid was filtered, washed with 3 L of water and 2.5 L of ethanol, and dried in a vacuum oven at 50° C. for 12 hours. Approximately 240 g of 3-mercapto-2-(4-methoxy-benzylamino)-propionic acid was obtained (68% yield). 1H NMR (300 MHz, DMSO) δ 7.32 (d, 8.9 Hz, 2H), 6.91 (d, 8.9 Hz, 2H), 3.87 (AB, JAB=13.1 Hz, ΔvAB=18.5 Hz, 2H), 3.72 (s, 3H), 3.24 (dd, J=5.3, 5.3 Hz, 1H), 2.76 (d, J=5.7 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414137B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-877ef83902694cdb91d20fd89cd52a55 |
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| Source note | uspto-grants-2008_08 |
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