HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491532Generated: October 31, 2026
2-Chloroethanol → 2-Chloroethyl 2-hydroxypropanoate
https://huagongshe.com/reaction/1491532
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Lactic Acid | HCID 612 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Chloroethyl 2-hydroxypropanoate | HCID 18953228 | 60% |
Reaction Steps
Lactic acid (74 mL of an 85% aqueous solution, 0.84 mol) and freshly distilled 2-chloroethanol (670 mL, 10.0 mol) were refluxed with 400 mL of toluene and 0.4 mL of conc. H2SO4 until one equivalent of H2O was collected in a Dean-Stark trap. The reaction mixture was cooled to room temperature, diluted with ethyl ether, and washed with a NaHCO3 /NaCl solution. The organic phase was dried with MgSO4, solvent was removed under reduced pressure, and the residue was distilled at 10 mm Hg. A fraction recovered at 95°-100° C./10 mm Hg was redistilled to give 2-chloroethyl lactate as a clear colorless liquid (76.7 g, 60%): b.p. 95° C./10 mm Hg; 1H NMR δ1.46 (d, 3H, J=6.9 Hz), δ2.95 (bs, 1H), δ3.72 (t, 2H, J=5.6 Hz), δ4.35 (q, 1H, J=6.9 Hz), δ4.44 (m, 2H); 13C NMR 20.4, 41.2, 64.8, 66.8, 175.2 ppm; HRMS calcd for C4H5ClO3Tms (M-CH3) 209.0401, obsd 209.0392.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05371001 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-ca21cf96df614efbb8dce68c408061ee |
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| Source note | uspto-grants-1994_12 |
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