Technology Process of (R)-4-[2-(cyclohex-1-en-1-yl)ethyl]-2,2-dimethyl-1,3-dioxolane
There total 2 articles about (R)-4-[2-(cyclohex-1-en-1-yl)ethyl]-2,2-dimethyl-1,3-dioxolane which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
(S)-4-(1,4-Dithia-spiro[4.5]dec-6-en-7-yl)-butane-1,2-diol;
With
potassium carbonate; 1,4-bis(9-O-dihydroquinidine)phthalazine; potassium hexacyanoferrate(III);
potassium osmate(VI); methanesulfonamide;
In
water; tert-butyl alcohol;
at 0 ℃;
2-Methoxypropene;
With
camphor-10-sulfonic acid;
In
N,N-dimethyl-formamide;
for 2h;
With
ammonia; sodium;
In
tetrahydrofuran;
at -78 ℃;
for 0.666667h;
Title compound not separated from byproducts;
DOI:10.1002/anie.200500513
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: (DHQD)2PYR; potassium ferricyanide; potassium carbonate / methanesulfonamide; potassium osmate / 2-methyl-propan-2-ol; H2O / 0 °C
2.1: (DHQD)2PHAL; potassium ferricyanide; potassium carbonate / methanesulfonamide; potassium osmate / 2-methyl-propan-2-ol; H2O / 0 °C
2.2: camphorsulfonic acid / dimethylformamide / 2 h
2.3: ammonia; sodium / tetrahydrofuran / 0.67 h / -78 °C
With
hydroquinindine-2,5-diphenyl-4,6-pyrimidinediyl diether; potassium carbonate; 1,4-bis(9-O-dihydroquinidine)phthalazine; potassium hexacyanoferrate(III);
potassium osmate(VI); methanesulfonamide;
In
water; tert-butyl alcohol;
1.1: Sharpless asymmetric dihydroxylation / 2.1: Sharpless asymmetric dihydroxylation;
DOI:10.1002/anie.200500513