(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL
(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Basic information
- Product Name:
- (1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL
- Synonyms:
-
- (1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL
- (1S)-TRANS-1,2-CYCLOHEXANEDIOL
- (1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL, 99% ( 99% EE/GLC)
- (1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL 98%
- (1S,2S)-1α,2β-Cyclohexanediol
- [1S,2S,(+)]-1,2-Cyclohexanediol
- (1S,2S)-trans-1,2-Cyclohexanediol,98%
- (S,S)-(+)-1,2-CYCLOHEXANEDIOL
- CAS:
- 57794-08-8
- MF:
- C6H12O2
- MW:
- 116.16
- Mol File:
- 57794-08-8.mol
(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Chemical Properties
- Melting point:
- 107-109 °C(lit.)
- Boiling point:
- 177.22°C (rough estimate)
- Density
- 0.9958 (rough estimate)
- refractive index
- 1.4270 (estimate)
- Flash point:
- 134 °C
- pka
- 14.49±0.40(Predicted)
- optical activity
- [α]20/D +39°, c = 1.6 in H2O
- BRN
- 1901343
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Usage And Synthesis
Chemical Properties
white to off-white crystals
Uses
(1S,2S)-trans-1,2-Cyclohexanediol may be used in the preparation of (1S,2S)-1,2-cyclohexanediyl bis(4-vinylbenzoate) by reacting with 4-vinylbenzoyl chloride. It may also be used as a chiral ligand for the preparation of non-racemic hydroxy phosphonates via titanium alkoxide-catalyzed addition of dimethyl phosphite to the corresponding aldehydes.
Purification Methods
The enantiomers have been recrystallised from *C6H6 or EtOAc. The (±) diol has been resolved via the distrychnine salt of the hemisulfate [Hayward et al. J Chem Soc Perkin Trans 1 2413 1976], or the 1-menthoxy acetates. {l-trans-diastereoisomer has m 64o, []D -91.7o (c 1.4 EtOH) from pet ether or aqueous EtOH and yields the (-)-trans-diol } and {d-trans-diastereoisomer has m 126-127o, []D -32.7o (c 0.8 EtOH) from pet ether or aqueous EtOH and yields the (+)-trans diol}. The bis-4-nitrobenzoate has m 126.5o []D (-) and (+) 25.5o (c 1.1 CHCl3), and the bis-3,5-dinitrobenzoate has m 160o []D ± 83.0o (c 1.8 CHCl3) [Wilson & Read J Chem Soc 1269 1935]. [Beilstein 6 III 4060.]
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