Olivetol

Olivetol

Names
IUPAC name 5-Pentyl-1,3-benzenediol
Other names 5-Pentylresorcinol; 5-n-Amylresorcinol
Identifiers
CAS Number	500-66-3 Y
ChEBI	CHEBI:66960 N
ChemSpider	9949 N
EC Number	207-908-8
Jmol 3D model	Interactive image
PubChem	10377
UNII	65OP0NEZ1P Y
InChI InChI=1S/C11H16O2/c1-2-3-4-5-9-6-10(12)8-11(13)7-9/h6-8,12-13H,2-5H2,1H3 N Key: IRMPFYJSHJGOPE-UHFFFAOYSA-N N InChI=1/C11H16O2/c1-2-3-4-5-9-6-10(12)8-11(13)7-9/h6-8,12-13H,2-5H2,1H3 Key: IRMPFYJSHJGOPE-UHFFFAOYAG
SMILES CCCCCC1=CC(=CC(=C1)O)O
Properties
Chemical formula	C11H16O2
Molar mass	180.25 g·mol−1
Melting point	40 to 41 °C (104 to 106 °F; 313 to 314 K) (49 to 49.5 °C)
Boiling point	162 to 164 °C (324 to 327 °F; 435 to 437 K) at 5 mmHg; 192-195 °C at 11 mmHg
Vapor pressure	{{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Olivetol, also known as 5-pentylresorcinol or 5-pentyl-1,3-benzenediol, is an organic compound found in certain species of lichen; it is also a precursor in various syntheses of tetrahydrocannabinol.

Occurrence

Olivetol is a naturally occurring organic compound. It is found in certain species of lichens and can be readily extracted.

5-Pentylresorcinol is also produced by a number of insects, either as a pheromone, repellent or antiseptic.

The cannabis plant internally produces the related substance olivetolic acid (OLA), which was hypothesized that the plant in turn utilizes to biosynthesize the psychoactive product tetrahydrocannabinol (THC).

Synthesis of products

This compound has been documented as being a usable ingredient in various methods of condensation reactions, which can produce a synthetic form of THC.

One such method is a condensation reaction of olivetol and pulegone. In PiHKAL, Shulgin also notes a cruder method of producing the same product by bringing to reaction olivetol and the essential oil obtained from orange peel in the presence of phosphoryl chloride. It can also be produced by reacting olivetol with α-pinene.

Another method for the stereospecific synthesis of Δ⁹-tetrahydrocannabinol comprising condensing olivetol with ²-carene oxide.

Legality

The production, possession and/or distribution of olivetol is not currently known to be outlawed by any country.

Biosynthesis

olivetol synthase

Olivetol is biosynthesized by a polyketide synthase-type reaction from hexanoyl-CoA and three molecules of malonyl-CoA by an aldol condensation of a tetraketide intermediate. In 2009, Taura et al. was able to clone a type III PKS named olivetol synthase (OLS) from Cannabis sativa. This PKS is a homodimeric protein that consists of a 385 amino acid polypeptide with a molecular mass of 42,585 Da that has high sequence similarity (60-70%) identity to plant PKS's.

The data from Taura’s study of OLS's enzyme kinetics show that OLS catalyzes a decarboxylative-aldol condensation to produce olivetol. This is similar to stilbene synthase’s (STS) mechanism for converting p-coumaroyl-CoA and malonyl-CoA to resveratrol. Although olivetol is the decarboxylated form of OLA, it is highly unlikely that OLS produces olivetol from OLA. Crude enzyme extracts prepared from flowers and leaves did not synthesize olivetolic acid, but only yielded olivetol. The exact mechanism of olivetol biosynthesis is as yet unsure, but it is possible that an OLA-forming metabolic complex forms along with OLS. In addition, it also appears that OLS only specifically accepts starter CoA esters with C4 to C8 aliphatic side chains such as hexanoyl-CoA.