HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379350Generated: October 25, 2026
Benzyl Chloride → Ethyl 2-benzyl-1,3-dithiane-2-carboxylate
https://huagongshe.com/reaction/1379350
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Ethyl 1,3-dithiane-2-carboxylate | HCID 88552 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-benzyl-1,3-dithiane-2-carboxylate | HCID 303709 | 88.5% |
Reaction Steps
A solution of 3.0 g (15.6 mmol) of 2-ethoxycarbonyl-1,3-dithiane in 40 ml of dry tetrahydrofuran was cooled under inert atmosphere to -78° C. and treated with 7.5 ml (15.6 mmol) of n-butyllithium. The resulting solution was warmed to -25° C., stirred for 20 min, recooled to -78° C., treated with 1.8 ml (15.6 mmol) of benzyl chloride, and stirred at ambient temperature for 16 h. After quenching with aqueous ammonium chloride, the mixture was extracted with ether, washed sequentially with water, aqueous sodium thiosulfate, and brine, dried over MgSO4, and concentrated in vacuo. Flash chromatography using 5% ethyl acetate in hexane gave 3.9 g (88%) of the desired compound. 1H NMR (CDCl3) δ 1.33 (t, J=7 Hz, 3H), 1.85 (qt, J=14, 3 Hz, 1H), 2.11 (dm, J=14 Hz, 1H), 2.69 (dt, J=14, 4 Hz, 2 H), 3.23 (ddd, J=14, 12, 3 Hz, 2H), 3.38 (s, 2H), 4.27 (q, J=7 Hz, 2H), 7.25-7.35 (m, 5H). Mass spectrum (M+NH4)+ =300.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05670675 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-702a12b08c19450ea39ebd6aabd4e4d8 |
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| Source note | uspto-grants-1997_09 |
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