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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713913Generated: October 29, 2026

Methyl 2-(hydroxymethyl)prop-2-enoate → HCID 178500921, compound

https://huagongshe.com/reaction/713913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(hydroxymethyl)prop-2-enoateHCID 11815329—
ReactantHCID 178445772HCID 178445772—
SolventMethanolHCID 887—
ProductHCID 178500921HCID 17850092158.5%

Reaction Steps

Compounds (6-((trans)-4-tert-butylcyclohexyloxy)naphthalen-2-yl)methanamine (311 mg, 1.0 mmol, 1.0 eq.) and methyl 2-(hydroxymethyl)acrylate (116 mg, 1.0 mmol, 1.0 eq.) was dissolved in MeOH (5 mL). The mixture was stirred at r.t. for 2 h. Then the mixture was concentrated and purified by silica gel column chromatography using DCM/CH3OH (10/1) to give product (250 mg, 58%) as a slight yellow oil. ESI-MS (M+H)+: 428.3. HPLC: 90.18%. 1H NMR (400 MHz, CDCl3) δ 7.68 (t, 2H), 7.63 (s, 1H), 7.37 (dd, 1H), 7.14-7.11 (m, 2H), 4.27-4.25 (m, 1H), 4.01-3.96 (m, 2H), 3.91 (s, 2H), 3.71 (s, 3H), 3.18-2.93 (AB, 2H), 2.73-2.71 (m, 1H), 2.28-2.25 (m, 2H), 1.90-1.87 (m, 2H), 1.45-1.40 (m, 2H), 1.25-1.09 (m, 3H), 0.89 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09186367B2
Source datasetuspto-grants-2015_11
ORD IDord-9260aa2e08af4e50a763fdfacd7f0dbc
Source noteuspto-grants-2015_11