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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537646Generated: October 29, 2026

Ethyl Lactate → Ethyl 2-benzyloxylactate

https://huagongshe.com/reaction/537646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl LactateHCID 7344—
ReactantCyclohexaneHCID 8078—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantBenzyl 2,2,2-trichloroacetimidateHCID 144968—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-benzyloxylactateHCID 18454908—

Reaction Steps

Trifluoromethanesulfonic acid (1.0 mL) was added gradually to a stirred mixture of ethyl lactate (8.90 g, 75 mmole), benzyl 2,2,2-trichloroacetimidate (22.7 g, 90 mmole), anhydrous cyclohexane (100 mL), and anhydrous dichloromethane (50 mL). The mixture was stirred overnight at room temperature under argon atmosphere. The mixture was filtered, and the filtrate was washed with saturated solution of sodium hydrogen carbonate (250 mL), and with distilled water (250 mL). Then, the solution was dried with anhydrous sodium sulfate and the solvents were distilled under reduced pressure using a rotary evaporator. The residue was subjected to fractional vacuum distillation giving 9.6 g of colorless product. NMR (CDCl3): 1.21 ppm (t, —CH2CH3, 3H), 1.32 ppm (d, —CH2—, 3H), 4.13 ppm (m, —CH— and —CH2CH3, 3H), 4.50 ppm (m, —CH2—, 2H), 7.32 ppm (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865149B2
Source datasetuspto-grants-2014_10
ORD IDord-6571be00eb5e4cb095785ecde2d44e3d
Source noteuspto-grants-2014_10