HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → 1,4-Dioxaspiro[4.5]decan-8-ylmethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,4-Dioxaspiro[4.5]decan-8-ylmethanol | HCID 10080838 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,4-Dioxaspiro[4.5]decan-8-ylmethyl methanesulfonate | HCID 9992301 | — |
Reaction Steps
To a solution of (1,4-dioxa-spiro[4.5]dec-8-yl)-methanol (1.0 g, 5.8 mmol, 1.0 eq.) and ethyldiisopropylamine (17 mL, 3.0 eq.) in methylene chloride (4 mL) at 0° C. was added dropwise MsCl (0.46 mL, 1.0 eq.) and the resulting mixture was warmed to room temperature and stirred for 2 h. The reaction was quenched by addition of sat. NaHCO3 and the separated aqueous phase was extracted with 3× methylene chloride and 4×EtOAc. The combined organic phase was dried over Na2SO4, filtered and concentrated to give a crude methanesulfonic acid 1,4-dioxa-spiro[4.5]dec-8-ylmethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07868002B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-999cd3399e14434a9034c78469177d36 |
| Source note | uspto-grants-2011_01 |