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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680337Generated: October 25, 2026

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

https://huagongshe.com/reaction/1680337

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 numberUS04272437
Source datasetuspto-grants-1981_06
ORD IDord-a98069384f194f889f0a923993f1e4d1
Source noteuspto-grants-1981_06