HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058751Generated: October 25, 2026
Hydrochloric Acid → 2-Propoxyethyl 4-Bromobenzenesulfonate
https://huagongshe.com/reaction/1058751
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Glycol monopropyl ether | HCID 17756 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Propoxyethyl 4-Bromobenzenesulfonate | HCID 22707936 | 48% |
Reaction Steps
To a solution of 2-propoxy-1-ethanol (1.5 g, 14.4 mmol) and triethylamine (2.2 g, 21.6 mmol) in dichloromethane (20 mL) at 0° C. was added 4-bromobenzenesulfonyl chloride (3.86 g, 15.1 mmol) in dichloromethane (10 mL) dropwise over 30 minutes. The reaction was then warmed to room temperature and stirred for 16 hours. The mixture was then poured into water (50 mL) and acidified with 2N aqueous hydrochloric acid (15 mL). The aqueous layer was extracted with dichloromethane and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to give a crude residue. This was purified by column chromatography on silica gel (50 g), eluting with hexane:ethyl acetate (9:3), to give the title compound (2.2 g, 48%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518282B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-c89d7cc853f34728b8f8c96a8a5e393d |
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| Source note | uspto-grants-2003_02 |
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