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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761370Generated: November 1, 2026

Benzyl Alcohol → HCID 15042555, compound

https://huagongshe.com/reaction/1761370

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 36. 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 36 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 numberUS04826815
Source datasetuspto-grants-1989_05
ORD IDord-9d27bb2ef399462ea0c896addee302b2
Source noteuspto-grants-1989_05