HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 2-((6-Chrysenylmethyl)amino)-2-methyl-1,3-propanediol diacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-((6-Chrysenylmethyl)amino)-2-methyl-1,3-propanediol hydrochloride | HCID 13375278 | — |
| Product | 2-((6-Chrysenylmethyl)amino)-2-methyl-1,3-propanediol diacetate | HCID 15599318 | 65.2% |
Reaction Steps
A mixture of 2-((6-chrysenylmethyl)amino)-2-methyl-1,3-propanediol hydrochloride (1B, 5.0 g, 13.1 mmol) and acetylchloride (Aldrich, 5.0 mL, 70.3 mmol) was refluxed in dry THF (200 mL) under N2 for 12 h. The reaction mixture was poured into a satd. NaHCO3 solution (500 mL) and extracted with EtOAc (3×500 mL). The EtOAc layes were combined, dried (K2CO3) and filtered to give a slightly yellow liquid. The solvent was removed to give an off-white solid. This was recrystallized 3× from PhCH3 /hexane (1:1). After filtration and drying, 3.67 g (65.2%) of 2-((6-chrysenylmethyl)amino)-2-methyl-1,3-propanediol diacetate was obtained mp 136°-137.5°, (C, H, N).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04810727 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-a80572704fd04888b602d3e288924eee |
| Source note | uspto-grants-1989_03 |