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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33574Generated: October 28, 2026

1-(2-Methoxynaphthalen-1-yl)-2-oxopropyl acetate → 1-Hydroxy-1-(2-methoxy-naphthalen-1-yl)-propan-2-one

https://huagongshe.com/reaction/33574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxynaphthalen-1-yl)-2-oxopropyl acetateHCID 14113550—
ReactantAcetic acid 2-(2-methoxy-naphthalen-1-yl)-1-methyl-2-oxo-ethyl esterHCID 59796867—
ProductHCID 59796849HCID 59796849—
Product1-Hydroxy-1-(2-methoxy-naphthalen-1-yl)-propan-2-oneHCID 5979687059%

Reaction Steps

2-hydroxy-1-(2-methoxy-naphthalen-1-yl)-propan-1-one and 1-hydroxy-1-(2-methoxy-naphthalen-1-yl)-propan-2-one (4.5:1 mixture) (580 mg, 59%) were prepared from acetic acid 1-(2-methoxy-naphthalen-1-yl)-2-oxo-propyl ester and acetic acid 2-(2-methoxy-naphthalen-1-yl)-1-methyl-2-oxo-ethyl ester (3:1 mixture) according to the method in Example 16A(c) as an orange solid, 1H NMR (CDCl3): 1.3 (3H, d, J=7.2 Hz), 2.0 (3H, s), 3.75 (1H, d, J=5.0 Hz), 3.9 (3H, s), 3.95 (3H, s), 4.2 (1H, d, J=3.5 Hz), 5.0 (1H, m), 5.9 (1H, d, J=3.5 Hz), 7.25-7.30 (2H, m), 7.35-7.40 (2H, m), 7.45-7.50 (2H, m), 7.6 (1H, d, J=7.7 Hz), 7.75 (2H, m), 7.85 (1H, d, J=9.0 Hz), 7.90-7.95 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429607B2
Source datasetuspto-grants-2008_09
ORD IDord-8c2444aeac334f92a1ac0bd9ad41b3a6
Source noteuspto-grants-2008_09