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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653872Generated: November 1, 2026

2-(Phenylmethyl)oxirane → HCID 22905182, compound

https://huagongshe.com/reaction/1653872

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, 0.186mol) 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05403836
Source datasetuspto-grants-1995_04
ORD IDord-cfb57e491c4d41cf9eb09186020a6224
Source noteuspto-grants-1995_04