HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39497Generated: October 26, 2026
Benzene → Dodecyl 2-chloro-3-hydroxypropionate
https://huagongshe.com/reaction/39497
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1-Dodecanol | HCID 8193 | — |
| Reactant | 2-Chloro-3-hydroxypropionic acid | HCID 564951 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Dodecyl 2-chloro-3-hydroxypropionate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524942B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-dd70758721d642d29d1cf230ba39a7bb |
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| Source note | uspto-grants-2013_09 |
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