Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39497Generated: October 26, 2026

Benzene → Dodecyl 2-chloro-3-hydroxypropionate

https://huagongshe.com/reaction/39497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1-DodecanolHCID 8193—
Reactant2-Chloro-3-hydroxypropionic acidHCID 564951—
SolventDichloromethaneHCID 6344—
ProductDodecyl 2-chloro-3-hydroxypropionateHCID 86651356—

Reaction Steps

2-chloro-3-hydroxypropionic acid (4.80 g, 0.03 mol), dodecanol (6.00 g, 0.03 mol) were taken with 5 mL dry benzene in a (50 mL) RB, with a dean-stark apparatus and condenser; 25 mg (0.26 mmol) para-Toluene sulfonic acid (pTSA) was added to it and the mixture was stirred at 75° C.-80° C. for 40 h. 1H-NMR showed 85% conversion. More 2-chloro-3-hydroxypropionic acid (1.00 g, 8.00 mmol) was added to it and heated at 75° C.-80° C. for 20 h. 1H-NMR showed almost complete conversion. After cooling it down, the product was added with 100 mL of CH2Cl2. Organic phase was washed twice with 50 mL of dil. NaHCO3 aq. sol. and once with 50 mL of sat. NaCl aq. sol. and then dried over anhy. Na2SO4. After filtration and removing the solvent by rotary evaporation, yield=7.76 g (78%). It was used for the next reaction without further purification. 1H-NMR (CDCl3, 7.27 ppm): 2.18-2.40 (broad, —OH), 3.97 (m, —CH2OH), 4.21 (m, —CO2CH2), 4.39 (m, —CHCl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524942B2
Source datasetuspto-grants-2013_09
ORD IDord-dd70758721d642d29d1cf230ba39a7bb
Source noteuspto-grants-2013_09