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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925238Generated: October 28, 2026

Benzyl Alcohol → benzyl N-(6-hydroxynaphthalen-2-yl)carbamate

https://huagongshe.com/reaction/1925238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
Reactant6-Hydroxy-2-naphthoic acidHCID 85557—
Reactant12-Deoxyphorbol 13-phenylacetate 20-acetateHCID 3034821—
SolventTolueneHCID 1140—
Productbenzyl N-(6-hydroxynaphthalen-2-yl)carbamateHCID 67520229—

Reaction Steps

6-Hydroxy-2-naphthoic acid (30 g, 160 mmol, Aldrich), dppa (48.4 g, 176 mmol, Aldrich), benzyl alcohol (51.8 g, 480 mmol, Aldrich) and Et3N (32.3 g, 320 mmol, Aldrich) were heated at reflux with toluene (500 mL, Aldrich) for 16 h. After cooling to RT, the volatile portion was removed in vacuo. The resulting brown residue was purified by silica gel column chromatography (40% EtOAc/hexane) to give crude compound, which was further purified by crystallization from 50% EtOAc/Hexane to give the title compound as an off-white solid. MS (ESI, pos. ion) m/z: 294.2 (M+1). Mass Calc'd for C18H15NO3: 293.11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178557B2
Source datasetuspto-grants-2012_05
ORD IDord-4acbdd224fdc4bd9a95b0f40a223000a
Source noteuspto-grants-2012_05