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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376644Generated: October 30, 2026

2-(Phenylmethyl)oxirane → HCID 22905182, compound

https://huagongshe.com/reaction/1376644

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 numberUS05663166
Source datasetuspto-grants-1997_09
ORD IDord-157327fba6434cbeac887084c3bd11ce
Source noteuspto-grants-1997_09