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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852570Generated: October 30, 2026

Benzyl Alcohol → Benzyl [1-(3-methoxyphenyl)-1-methylethyl]carbamate

https://huagongshe.com/reaction/852570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-(3-Methoxyphenyl)-2-methylpropanoic acidHCID 10821634—
SolventTolueneHCID 1140—
ProductBenzyl [1-(3-methoxyphenyl)-1-methylethyl]carbamateHCID 6726426665%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-(3-methoxy-phenyl)-2-methyl-propionic acid (D99) (1 g, 5.15 mmol, 1 equiv) in toluene (20 ml) at room temperature was added NEt3 (1.07 ml, 7.72 mmol, 1.5 equiv) and then diphenylphosphoryl azide (2.2 ml, 10.3 mmol, 2 equiv). The resulting mixture was then heated at 80° C. for 2 h then benzyl alcohol (1.61 ml, 15.45 mmol, 3 equiv) was added and the solution heated for a further 2 h, cooled to room temperature and partitioned between EtOAc and a saturated NaHCO3 aqueous solution. The two layers were separated and the aqueous phase dried over MgSO4 and concentrated. in vacuo. Purification of the residue by flash chromatography on silica gel (iso-hexane/AcOEt: 9/1) gave [1-(3-methoxy-phenyl)-1-methyl-ethyl]-carbamic acid benzyl ester (D100) (1 g, 65%) a yellow gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-4e52f4e85cd94b1f8b7201628d1121fe
Source noteuspto-grants-2007_08