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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355239Generated: October 24, 2026

Triethylamine → (1R,2R)-ethyl 2-((methylsulfonyloxy)methyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/355239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEthyl (1R,2R)-2-(hydroxymethyl)cyclopropanecarboxylateHCID 29920784—
SolventTetrahydrofuranHCID 8028—
Product(1R,2R)-ethyl 2-((methylsulfonyloxy)methyl)cyclopropanecarboxylateHCID 53825740—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of trans-ethyl 2-hydroxymethyl-1-cyclopropanecarboxylate (1.136 g, 7.88 mmol) in dry tetrahydrofuran (20 ml) was cooled to 0° C. (ice bath), treated dropwise with mesyl chloride (0.675 ml, 8.66 mmol) and then treated immediately with triethylamine (1.32 ml, 9.52 mmol). This solution was stirred at 0° C. for 1.5 h (tlc indicated no substrate left). After dilution with ether (200 ml), the solution was washed with water, saturated ammonium chloride (10 ml), brine and dried over anhydrous magnesium sulfate. Evaporation of the solvent under reduced pressure gave a clear oil, 1.690 g (97%) which was used as such for the next step without purification. ir (film) νmax : 1720 cm-1 (C=O); 1Hmr (CDCl3) δ: 4.13 (2H, q, J=7, CH2 --CH3, 3.05 (2H, s, CH2 --OMs), 2.0~0.6 (4H, m, cyclopropyl), 1.27 ppm (3H, t, J=7, CH3 --CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04378314
Source datasetuspto-grants-1983_03
ORD IDord-41c9eeaee4d84aefa6df148d6cab7119
Source noteuspto-grants-1983_03