HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716142Generated: October 30, 2026
Hydrochloric Acid → HCID 131734120, compound
https://huagongshe.com/reaction/716142
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 131734119 | HCID 131734119 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131734120 | HCID 131734120 | — |
Reaction Steps
0.35 mL of methanesulfonyl chloride was added dropwise to a solution of 1.5 g of 1-benzyloxy-5-((triisopropyl)silyloxy)pentan-2-ol and 0.7 mL of triethylamine in 15 mL of ethyl acetate at a temperature of 5° C. to 10° C., and the obtained mixture was then stirred at room temperature for 1 hour. Thereafter, the reaction mixture was added to a mixture of 100 mL of ethyl acetate and 50 mL of 1 mol/L hydrochloric acid. The organic layer was fractionated. The obtained organic layer was successively washed with 50 mL of a saturated sodium hydrogen carbonate aqueous solution, 50 mL of water and 50 mL of a saturated sodium chloride aqueous solution, and it was then dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure, so as to obtain 1.8 g of 1-benzyloxy-5-((triisopropyl)silyloxy)pentan-2-yl methanesulfonate in the form of a colorless oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09187514B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-c7779d78de1c453da69813ca57111dd1 |
|---|
| Source note | uspto-grants-2015_11 |
|---|