HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49328Generated: October 26, 2026
Triethylamine → 5-(2-Ethyl-[1,3]dioxolan-2-yl)-2-thienylmethyl methanesulphonate
https://huagongshe.com/reaction/49328
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | [5-(2-Ethyl-[1,3]dioxolan-2-yl)-2-thienyl]methanol | HCID 17934796 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(2-Ethyl-[1,3]dioxolan-2-yl)-2-thienylmethyl methanesulphonate | HCID 20636301 | — |
Reaction Steps
9.25 g (43.2 mmol) of [5-(2-ethyl-[1,3]dioxolan-2-yl)-2-thienyl]methanol are dissolved in 500 mL of dichloromethane and cooled to 0° C. 9.0 mL (64.7 mmol) of triethylamine are added, followed by 3.5 mL of methylsulphonyl chloride (45.3 mmol). After stirring for 1 hour, the reaction medium is treated with ammonium chloride solution and extracted with dichloromethane. The organic phases are combined, dried and concentrated under reduced pressure. A brown oil is obtained (m=9.28 g; Y=75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706725B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-1df85117b94e458c8d44dd2cbc29df2c |
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| Source note | uspto-grants-2004_03 |
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