HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453766Generated: October 30, 2026
Hydrochloric Acid → (R)-(6-(benzyloxy)-2,3-dihydrobenzo[b][1,4]dioxin-2-yl)methyl methanesulfonate
https://huagongshe.com/reaction/453766
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | ((S)-6-Benzyloxy-2,3-dihydrobenzo[1,4]dioxin-2-yl)methanol | HCID 66726995 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-(6-(benzyloxy)-2,3-dihydrobenzo[b][1,4]dioxin-2-yl)methyl methanesulfonate | HCID 86644715 | — |
Reaction Steps
To a stirred solution of crude ((S)-6-benzyloxy-2,3-dihydrobenzo[1,4]dioxin-2-yl)methanol (1.65 g, 6.06 mmol) in dry DCM (10 ml), was added triethylamine (0.88 ml). The mixture was cooled to 0° C. and methanesulfonyl chloride (0.49 ml) was added slowly dropwise to reaction mixture. The mixture was stirred at RT for 1 h and then 10 ml of aq 1 M HCl was added. The mixture was extracted twice with DCM. The combined organic layers were washed with water and brine, dried with Na2SO4 The solvents were removed under reduced pressure and the crude product (2.22 g) was crystallized from IPA (15 ml), which gave a white solid (1.50 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492549B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-93b25e03a0fd4a67a94454af19b7d1d8 |
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| Source note | uspto-grants-2013_07 |
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