99107-52-5 Usage
Originator
Bunaprolast,ZYF Pharm Chemical
Manufacturing Process
Preparation of pentacarbonyl[phenyl(methoxy)carbene]chromium:
To a suspension of 22 g (0.1 mole) of chromium hexacarbonyl in ether is
slowly added phenyllithium (51 ml, 0.1 mole, cyclohexane/ether solution) via
syringe over a period of 15-20 minutes under argon at room temperature, and
the resulting deep red solution is stirred at room temperature for 1 hour. The
solvent is removed under reduced pressure (bath temperature should be
below 40°C), and the black residue is dissolved in 200 ml water. (CH3)3O·BF4
(about 15 g) is added portionwise to the solution until it becomes slightly
acidic (pH 5.5). The aqueous layer is extracted three times with 200 ml of
ether, and the combined etheral extracts are washed once with 300 ml of
saturated brine solution, once with 300 ml of saturated sodium carbonate
solution, and three times with 300 ml of saturated brine solution, dried over
anhydrous sodium sulfate and filtered. The solvent is removed using a rotary
evaporator. The deep red tarry residue is purified using flash chromatography
by a silica gel column (200 g). Elution by 10% ether in n-hexane gives a deep
red syrup, which is solidified upon cooling. Recrystallization from pet-ether at
-70°C gives 25.12 g (80.5%) of pentacarbonyl[phenyl(methoxy)carbene]
chromium as deep red crystalline. The physical properties of the product are
consistent with those described in the literature.
2-Butyl-4-methoxy-1-naphthalenol, acetate:
Reaction of pentacarbonyl[phenyl(methoxy)carbene ]chromium with 1-
hexyne:
Part A.
A mixture of the carbene complex (1.0 g, 3.2 mmole), 1-hexyne (2.6
equivalents), acetic anhydride (1.0 eq.) and triethylamine (1.0 eq.) in
tetrahydrofuran (90 ml) is heated at 65°C under an argon atmosphere for 1
hour. The solution is cooled and concentrated to give a black residue, which is
chromatographed through a silica gel (200 g) column using a flash
chromatography. Elution by10% ether in n-hexane gives 71 5 mg (82.2%) of
the title product, which solidified. Recrystallization from pet-ether gave white
crystals of 2-butyl-4-methoxy-1-naphthalenol acetate; MP: 49°C.
Part B.
Alternatively, a mixture of 2.0 g (6.4 mmole) of the carbene complex,
acetylene (2.6 eq.) and acetic acid in tetrahydrofuran is heated at 65°C for 2
hours under argon atmosphere. After cooling the reaction solution is
concentrated and the black residue is loaded on a silica gel (200 g) column for
a flash chromatography. Elution by 10% ether in n-hexane gives 895 mg
(51.4%) of the title product.
Check Digit Verification of cas no
The CAS Registry Mumber 99107-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,1,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99107-52:
(7*9)+(6*9)+(5*1)+(4*0)+(3*7)+(2*5)+(1*2)=155
155 % 10 = 5
So 99107-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H20O3/c1-4-5-8-13-11-16(19-3)14-9-6-7-10-15(14)17(13)20-12(2)18/h6-7,9-11H,4-5,8H2,1-3H3
99107-52-5Relevant academic research and scientific papers
REACTION OF ARYL CHROMIUM CARBENE COMPLEXES WITH 1-HEXYNE; FORMATION OF UNUSUAL DIELS-ALDER CYCLOADDITION PRODUCTS
Yamashita, A.,Timko, J.M.,Watt, W.
, p. 2513 - 2516 (2007/10/02)
The reaction of an aryl chromium carbene complex with 1-hexyne provided a benzannualated product as a major component along with unusual Diels-Alder cycloaddition products.
