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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655699Generated: November 1, 2026

2-(Phenylmethyl)oxirane → HCID 22905182, compound

https://huagongshe.com/reaction/1655699

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Phenylmethyl)oxiraneHCID 94826—
ReactantProp-1-en-1-amineHCID 53650673—
SolventMethanolHCID 887—
ProductHCID 22905182HCID 22905182101.7%

Reaction Steps

A solution of 1-aminopropylene (10.6 grams, 0.186 mol) in methanol was added to a methanolic solution of 3-phenylpropyleneoxide (5.07 grams, 0.037 mol) 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250679
Source datasetuspto-grants-1993_10
ORD IDord-c5b7bbc6cfe34390b1500d2e52894378
Source noteuspto-grants-1993_10