Isoborneol

Isoborneol
Names

IUPAC name (1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-ol, (1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-ol
Identifiers
CAS Number	+: 16725-71-6 d -: 10334-13-1 rac: 124-76-5
3D model (JSmol)	+: Interactive image -: Interactive image rac: Interactive image
ChEBI	+: CHEBI:191949
ChEMBL	+: ChEMBL4294644 -: ChEMBL3560760
ChemSpider	+: 16739225 -: 4882019
PubChem CID	+: 6973640 -: 6321405
UNII	+: 8GDX32M6KF -: 20U67Z994U rac: L88RA8N5EG
UN number	1312
InChI +: InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m0/s1 Key: DTGKSKDOIYIVQL-OYNCUSHFSA-N -: InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m1/s1 Key: DTGKSKDOIYIVQL-MRTMQBJTSA-N
SMILES +: C[C@]12CC[C@H](C1(C)C)C[C@@H]2O -: C[C@@]12CC[C@@H](C1(C)C)C[C@H]2O rac: CC1(C2CCC1(C(C2)O)C)C
Properties
Chemical formula	C₁₀H₁₈O
Molar mass	154.253 g·mol⁻¹
Appearance	white or colorless solid
Melting point	212–214 °C (414–417 °F; 485–487 K) + or -; 210–215 °C for rac
Hazards
GHS labelling:^[1]
Pictograms
Signal word	Warning
Hazard statements	H228
Precautionary statements	P210, P240, P241, P280, P370+P378
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Isoborneol is a bicyclic organic compound and a terpene derivative. The hydroxyl group in this compound is placed in an exo position. The endo diastereomer is called borneol. Being chiral, isoborneol exists as enantiomers.

Preparation

Isoborneol is synthesized commercially by hydrolysis of isobornyl acetate. The latter is obtained from treatment of camphene with acetic acid in the presence of a strong acid catalyst.^[2]

It can also be produced by reduction of camphor:

Derivatives of isoborneol are used as ligands in asymmetric synthesis.^[3]

(2S)-(−)-3-exo-(morpholino)isoborneol or MIB^[4] with a morpholine substituent in the α-hydroxyl position.
(2S)-(−)-3-exo-(dimethylamino)isoborneol or DAIB^[5] with a dimethylamino substituent in the α-hydroxyl position

^ "(+)-Isoborneol". pubchem.ncbi.nlm.nih.gov. Retrieved 1 December 2022.
^ Sell, Charles S. (2006). "Terpenoids". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.2005181602120504.a01.pub2. ISBN 0471238961.
^ Yus, Miguel; Ramón, Diego (2007). "Chiral Ligands with an Isoborneol-10-sulfonamide Structure: A Ten-Year Odyssey". Synlett. 2007 (15): 2309–2320. doi:10.1055/s-2007-985602.
^ Chen, Y. K.; Jeon, S.-J.; Walsh, P. J.; Nugent, W. A. (2005). "(2S)-(−)-3-exo-(Morpholino)isoborneol". Organic Syntheses. 82: 87. doi:10.15227/orgsyn.082.0087.
^ White, J. D.; Wardrop, D. J.; Sundermann, K. F. (2002). "(2S)-(−)-3-exo-(Dimethylamino)isoborneol". Organic Syntheses. 79: 130. doi:10.15227/orgsyn.079.0130.

This page was last edited on 1 December 2022, at 10:02