HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Phenylmethyl)oxirane → HCID 22905182, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Phenylmethyl)oxirane | HCID 94826 | — |
| Reactant | Prop-1-en-1-amine | HCID 53650673 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22905182 | HCID 22905182 | 101.7% |
Reaction Steps
A solution of 1-aminopropylene (10.6 grams, 0.186mol) in methanol was added to a methanolic solution of 3-phenylpropyleneoxide (5.07 grams, 0.037mol) and the mixture heated to reflux for 30 minutes. The mixture was allowed to warm to room temperature and concentrated in vacuo to yield 7.2 grams (99%) of N-allyl-3-phenyl-2-hydroxypropylamine. 1H NMR (CDCl3, dTMS) 7.34-7.18 (5H, m, Ar--H), 5.84 (1H, ddt, 3JHH =17.1 Hz, 3JHH =10.2 Hz, 3JHH =6 Hz, CH2CH), 5.2-5.0 (2H, m, CH=CH2 ), 3.86 (1H, m, CHOH), 3.19 (2H, m, NCH2CH=CH2), 2.76-2.66 (3H, m, NCH2CH(OH)CHHPh), 2.50 (1H, dd 2JHH =12 Hz, 3JHH =9 Hz). 13C NMR (CDCl3) 138.4, 136.5, 129.3, 128.4, 126.3, 116.0, 70.6, 54.0, 51.9, 41.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05403836 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-cfb57e491c4d41cf9eb09186020a6224 |
| Source note | uspto-grants-1995_04 |