HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964820Generated: November 1, 2026
2-Chloroethanol → 2-Chloroethyl 3-hydroxybenzoate
https://huagongshe.com/reaction/964820
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | 3-Hydroxybenzoic Acid | HCID 7420 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloroethyl 3-hydroxybenzoate | HCID 15158791 | 95.2% |
Reaction Steps
##STR32## A solution of 3-hydroxybenzoic acid (15.0 g, 0.11 mol) in 2-chloroethanol (70 mL, 1.0 mol) and 1 mL of concentrated sulfuric acid was refluxed for overnight. TLC analysis (silica gel/20% ethyl acetate/hexane) showed clean conversion to a new material. The excess chloroethanol was removed by evaporation to obtain a brown solution which -was dissolved in ethyl acetate and washed with water. The organic layer was dried with MgSO4 and concentrated to obtain 21.0 g of the product as a white solid: mp 50° C.; 1H NMR (CDCl3) δ 3.81 (t, 2H, J=5.9 Hz), 4.57 (t, 2H, J=5.9 Hz), 4.77 (s, 1H), 7.06-7.66 (m, 4H), 13C NMR (CDCl3) δ 41.52, 64.75, 116.43, 120.77, 121.98, 129.80, 130.71, 156.04, 166.57; MS m/e (rel. intensity) 200 (26), 138 (59), 121 (100), 93 (31), 65 (21), 39 (12); MS exact mass; calcd. 200.0240, found 200.0242.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05770743 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-a85f7bd1892843d0a6b9a7793cc65b09 |
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| Source note | uspto-grants-1998_06 |
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