ChemicalBook--->CAS DataBase List--->41248-23-1

41248-23-1

41248-23-1 Structure

41248-23-1 Structure
IdentificationBack Directory
[Name]

ETHYL 1-HYDROXYCYCLOPENTANE-CARBOXYLATE
[CAS]

41248-23-1
[Synonyms]

ETHYL2-HYDROXYCYCLOPENTANE
ETHYL 1-HYDROXYCYCLOPENTANE-CARBOXYLATE
hydroxycyclopentanecarboxylic acid ethyl ester
1-Hydroxycyclopentanecarboxylic acid ethyl ester
1-hydroxy-1-cyclopentanecarboxylic acid ethyl ester
Cyclopentanecarboxylic acid, 1-hydroxy-, ethyl ester
[EINECS(EC#)]

201-215-5
[Molecular Formula]

C8H14O3
[MDL Number]

MFCD06797660
[MOL File]

41248-23-1.mol
[Molecular Weight]

158.2
Chemical PropertiesBack Directory
[Boiling point ]

206℃
[density ]

1.144
[Fp ]

77℃
[storage temp. ]

2-8°C
[form ]

liquid
[pka]

13.28±0.20(Predicted)
[color ]

Yellow
[InChI]

InChI=1S/C8H14O3/c1-2-11-7(9)8(10)5-3-4-6-8/h10H,2-6H2,1H3
[InChIKey]

GINOXNRTFZITQJ-UHFFFAOYSA-N
[SMILES]

C1(O)(C(OCC)=O)CCCC1
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2906190090
Hazard InformationBack Directory
[Uses]

Ethyl 1-hydroxycyclopentanecarboxylate, is a building block used in synthesis of variious compounds such as spiromesifen (S683505), a useful insecticide and miticide in plant breeding. Also useful in cannabis testing kits as a component of pesticide mixes (P698240).
[Synthesis]

1-Hydroxycyclopentanecarboxylic acid.

16841-19-3

Ethanol

64-17-5

ETHYL 1-HYDROXYCYCLOPENTANE-CARBOXYLATE

41248-23-1

Concentrated sulfuric acid (catalytic amount) was added slowly to a solution of 1-hydroxycyclopentanecarboxylic acid (0.98 g, 7.5 mmol) in ethanol (3.8 mL). The reaction mixture was stirred at room temperature for 3 days. Upon completion of the reaction, the solvent was removed by concentration under reduced pressure by rotary evaporator. The residue was dissolved in ethyl acetate (75 mL) and washed with saturated saline (25 mL). After separation of the organic layer, the aqueous layer was extracted once more with ethyl acetate (75 mL). All organic layers were combined and dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure to give 1-ethoxycarbonyl-1-cyclopentanol (1.13 g, 95% yield) as a light brown oil. The mass spectrum (MS) showed m/z: 159 ([M + H]+).

[References]

[1] Patent: WO2015/124541, 2015, A1. Location in patent: Page/Page column 81
[2] Patent: CN106432163, 2017, A. Location in patent: Paragraph 0053-0055
[3] Journal of the Chemical Society, 1934, p. 946,954
[4] Collection of Czechoslovak Chemical Communications, 1963, vol. 28, p. 2520 - 2523
[5] Chimia, 2003, vol. 57, # 11, p. 697 - 701
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