HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234174Generated: October 25, 2026
Chloride → tert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonate
https://huagongshe.com/reaction/234174
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloride | HCID 312 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | chloride (4R-cis)-6-(chloromethyl)-2,2-dimethyl-1,3-dioxane-4-acetic acid, 1,1-dimethylethyl ester | HCID 86747487 | — |
| Catalyst | Tetrabutylammonium Benzoate | HCID 10981353 | — |
| Product | tert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonate | HCID 9816650 | — |
Reaction Steps
Solid tetrabutylammonium benzoate obtained as above (126.47 g, 0.348 mole) was added in one portion to a mechanically stirred solution of the chloride (4R-cis)-6-(chloromethyl)-2,2-dimethyl-1,3-dioxane-4-acetic acid, 1,1-dimethylethyl ester prepared as in step (d) of Example 1 above (32.3 g, 0.116 mole) in HPLC grade 1-methyl-2-pyrrolidinone (465 ml) under argon. The resulting solution was stirred at 100° C. (internal temperature). After 30 to 60 minutes the reaction mixture became homogeneous and brown in color. The progress of the reaction was followed by TLC and GC analysis (TLC: Rf =0.47 for the chloride starting material; Rf =0.35 for the title compound (silica gel, Ether: Hexane, 4:6, visualization by Ce (SO4 )2 spray). After 6.5 hours the reaction was completed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05594153 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-6dd940ca42dd45989204e25a34732a24 |
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| Source note | uspto-grants-1997_01 |
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