HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465677Generated: October 30, 2026
HCID 11054393, compound → 2,3:5,6-Di-O-isopropylidene-D-mannono-1,4-lactone
https://huagongshe.com/reaction/465677
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 11054393 | HCID 11054393 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3:5,6-Di-O-isopropylidene-D-mannono-1,4-lactone | HCID 9943092 | — |
Reaction Steps
A solution of 2,3:5,6-di-O-isopropylidene-D-mannofuranose (diacetone mannose) (20 g, 76.9 mmol) in dichloromethane (100 ml) was added to a solution of pyridinium chlorochromate (33.2 g, 2.0 equiv) and dry powdered molecular sieve (40 g) in dichloromethane (300 ml) at 0° C. under nitrogen. The reaction mixture was stirred at room temperature for 30 min [when TLC (ether:hexane, 2:1) showed no starting material (Rf 0.36) and one major product (Rf 0.24)], diluted with ether (400 ml) and filtered through a silica plug. The silica plug was washed with ether and the filtrates were combined and the solvents removed to give, after recrystallization from ether, 2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone (11), (18.0 g, 90%), m.p. 125°-126° C. [lit. m.p. 125°-125° C.; Ohle et al., Chem. Ber. 58, 2590 (1925); Goodyear and Haworth, J. Chem. Soc. 1927, 3136⟧
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05153325 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-65e0a0ae4c2e498eaa6e89b482f85639 |
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| Source note | uspto-grants-1992_10 |
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