Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | methyl 3-thien-3-yipropionate | HCID 9793962 | — |
| Product | HCID 59855504 | HCID 59855504 | 87% |
Reaction Steps
A solution of 3-thiolpropanoic acid methyl ester (1.2 g, 10 mmol) and 4-bromobenzyl-bromide (2.5 g, 10 mmol) in DMF (20 mL) was cooled to 0° C. and treated with Cs2CO3 (3.9 g, 12 mmol). After stirred for 2 h, the reaction was quenched with 5% HCl (25 mL) and diluted with ethyl acetate (50 mL). After seperation, the aqueous layer extracted with ethyl acetate (3×15 mL). The combined organic layers were washed with sat. aq NaCl, dried over MgSO4 and concentrated. Purification by flash column chromatography (2-5% ethyl acetate in heptane) provided 3-(4-bromophenylmethylsulfanyl)-propanoic acid methyl ester (2.5 g, 87%) as white solid. 1H NMR (CDCl3), 7.43 (d, J=8 Hz, 2 H), 7.20 (d, J=8 Hz, 2 H), 3.68 (s, 5 H), 2.67 (m, 2 H), 2.56 (t, J=6 Hz, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07465825B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-5d99a4976d834c7ca9110fd3bdc99718 |
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| Source note | uspto-grants-2008_12 |
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