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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722675Generated: November 2, 2026

Benzyl Alcohol → HCID 15042555, compound

https://huagongshe.com/reaction/1722675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant4-Methoxy-3,3-dimethyl-4-oxobutanoic acidHCID 15039565—
SolventTolueneHCID 1140—
ProductHCID 15042555HCID 15042555—

Reaction Steps

3-Carbomethoxy-3-methylbutanoic acid [Bull. Soc. Chim. Fr., 828 (1965), 7.85 g, 0.049 mol]was reacted with diphenylphosphorylazide and triethylamine as described in Example 102. After heating the toluene solution for 1.5 h, benzyl alcohol (8 g) was added directly to the reaction mixture and heating at reflux was continued for 20 h. Work-up and chromatography gave methyl 3-benzyloxycarbonylamino-2,2-dimethylpropionate. NMR (300 MHz, CDCl3): 1.2 (s,6H), 3.3 (d,2H), 3.68 (s,3H), 5.1 (s,2H), 5.22 (m,1H). A sample of the methyl ester (6.21 g, 0.023 mol) was saponified with 3.1 g (0.78 mol) of NaOH in 100 ml ethanol/10 ml H2O at room temperature for 48 h. Work-up as in Example 102 gave the desired product as a liquid. NMR (300 MHz, CDCl3): 1.23 (s,6H), 3.32 (d,2H), 5.10 (s,2H), 5.27 (m,1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857507
Source datasetuspto-grants-1989_08
ORD IDord-90534470336b466d9f6a717d90381cdf
Source noteuspto-grants-1989_08