HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 22323657, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloro-1-propanol | HCID 12313 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22323657 | HCID 22323657 | 96.6% |
Reaction Steps
To 3-chloro-1-propanol (5.02 mL, 60 mmole) in CH3CN (200 mL) was added methanesulfonyl chloride (10.4 g, 90 mmole) and triethyl amine (13 mL, 90 mmole). The reaction mixture was stirred at room temperature for 12 hours under an argon atmosphere. 200 mL of saturated NaHCO3 (aq) was added and the stirring was continued for 15 minutes. The mixture was extracted several times with ether. The combined ether layers were dried over Na2SO4, the Na2SO4 was filtered and the filtrate was evaporated to give 10 g (96.6%) of the title compound: TLC (Rf: 0.3; 20% EtOAc/Hexane), 1H NMR (CDCl3) δ 2.2 (m, 2 H, CH2), 3.0 (s, 3 H, CH3), 3.6 (t, 2 H, CH2), 4.4 (t, 2 H, CH2). 13C NMR (CDCl3): δ 31.5 (CH2), 37.0 (CH3), 40.2 (CH2), 66.3 (CH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06121433 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-14d3c68a57fb488eb8532eab163b5213 |
| Source note | uspto-grants-2000_09 |