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Gamma-phenyl-gamma-butyrolactone, also known as GPBL, is a chemical compound with the molecular formula C11H12O2. It is a cyclic ketone derivative, featuring a phenyl group attached to a gamma-butyrolactone ring. This white crystalline solid is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of sedatives, hypnotics, and tranquilizers. GPBL is known for its reactivity and can undergo a range of chemical transformations, making it a versatile building block in organic chemistry. It is typically synthesized through the intramolecular cyclization of phenylbutyric acid derivatives. Due to its potential applications in the creation of psychoactive substances, GPBL is subject to regulatory controls in some jurisdictions.

69814-97-7

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69814-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69814-97-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,1 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69814-97:
(7*6)+(6*9)+(5*8)+(4*1)+(3*4)+(2*9)+(1*7)=177
177 % 10 = 7
So 69814-97-7 is a valid CAS Registry Number.

69814-97-7Relevant academic research and scientific papers

ENZYMATIC LACTONISATION OF γ-HYDROXYESTERS IN ORGANIC SOLVENTS. SYNTHESIS OF OPTICALLY PURE γ-METHYLBUTYROLACTONES AND γ-PHENYLBUTYROLACTONE.

Gutman, Arie L.,Zuobi, Kheir,Boltansky, Aviv

, p. 3861 - 3864 (1987)

Porcine pancreatic lipase in anhydrous organic solvents catalyses the lactonisation of a number of esters of γ-hydroxyacids in nearly quantitative yields.This enzymatic process was used for the highly stereoselective synthesis of (S)-(-)-γ-methylbutyrolactone, (R)-(+)-γ-methylbutyrolactone and of optically active γ-phenylbutyrolactone.

Synthesis and chiral recognition of helical poly(phenylacetylene)s bearing L-phenylglycinol and its phenylcarbamates as pendants

Zhang, Chunhong,Wang, Hailun,Yang, Taotao,Ma, Rui,Liu, Lijia,Sakai, Ryosuke,Satoh, Toshifumi,Kakuchi, Toyoji,Okamoto, Yoshio

, p. 809 - 821 (2015/03/04)

A series of novel stereoregular one-handed helical poly(phenylacetylene) derivatives (PPA-1 and PPA-1a-g) bearing L-phenylglycinol and its phenylcarbamate residues as pendants was synthesized for use as chiral stationary phases (CSPs) for HPLC, and their chiral recognition abilities were evaluated using 13 racemates. The phenylcarbamate residues include an unsubstituted phenyl, three chloro-substituted phenyls (3-Cl, 4-Cl, 3,5-Cl2), and three methyl-substituted phenyls (3-CH3, 4-CH3, 3,5-(CH3)2). The acidity of the phenylcarbamate N-H proton and the hydrogen bonds formed between the N-H groups of the phenylcarbamate residues were dependent on the type, position, and the number of substituents on the phenylcarbamate residues. The chiral recognition abilities of these polymers significantly depended on the dynamic helical conformation of the main chain with more or less regularly arranged pendants. The chiral recognition abilities seem to be improved by the introduction of substituents on the phenylcarbamate residues, and PPA-1d bearing the more acidic N-H groups due to the 3,5-dichloro substituents, exhibited a higher chiral recognition than the others. PPA-1d showed an efficient chiral recognition for some racemates, and baseline separation was possible for racemates 5, 11, 12, and 15.

Regio- and enantioselective Baeyer-Villiger oxidation: Kinetic resolution of racemic 2-substituted cyclopentanones

Zhou, Lin,Liu, Xiaohua,Ji, Jie,Zhang, Yuheng,Wu, Wangbin,Liu, Yangbin,Lin, Lili,Feng, Xiaoming

supporting information, p. 3938 - 3941 (2014/08/18)

A kinetic resolution of racemic 2-substituted cyclopentanones via highly regio- and enantioselective Baeyer-Villiger oxidation has been successfully developed. The reaction could afford the normal 6-substituted δ-lactones in up to 98% ee and >19/1 regioselectivity. Meanwhile, the unreacted ketones were recovered in excellent ee values (up to 98%). It represents the best results of the kinetic resolution of racemic 2-substituted cyclopentanones via nonenzymic asymmetric BV oxidation.

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