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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904212Generated: November 2, 2026

Benzyl Alcohol → HCID 15042555, compound

https://huagongshe.com/reaction/1904212

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 75. 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 purification as in Example 75 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, 0.23 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 75 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 numberUS04837204
Source datasetuspto-grants-1989_06
ORD IDord-44dda5db9bac4c77b1f35a15f8887f18
Source noteuspto-grants-1989_06