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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantEthyl 1,3-dithiane-2-carboxylateHCID 88552—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-benzyl-1,3-dithiane-2-carboxylateHCID 30370988.5%

Reaction Conditions

Temperature-25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670675
Source datasetuspto-grants-1997_09
ORD IDord-702a12b08c19450ea39ebd6aabd4e4d8
Source noteuspto-grants-1997_09