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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434701Generated: October 29, 2026

10-hydroxyimino-5-methylene-10,11-dihydro-5H-dibenzo[a,d]cycloheptene → HCID 12533738, compound

https://huagongshe.com/reaction/434701

Reaction equation

Participants

RoleNameHCIDCharge
Reactant10-hydroxyimino-5-methylene-10,11-dihydro-5H-dibenzo[a,d]cyclohepteneHCID 826704—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductHCID 12533738HCID 12533738—

Reaction Steps

A mixture of 15.3 of oxime from Step D, 500 ml of methanol, 12 g of sodium cyanoborohydride in 450 ml of methanol was treated dropwise with a solution of 12 ml of 12N hydrochloric in 50 ml of methanol over 5 hours, and then stirred overnight at room temperature. The solvent was evaporated, the residue was stirred with 200 ml of 1N aqueous hydrochloric acid, made alkaline with concentrated ammonium hydroxide and extracted with 3×175 ml of ether. The combined extracts were dried (Na2SO4), filtered and evaporated. The crystalline residue was washed with methanol to give 9.6 g of 10-hydroxamino-5-methylene-10,11-dihydro-5H-dibenzo[a,d]cyclohepten, m.p. 145°-147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399141
Source datasetuspto-grants-1983_08
ORD IDord-e06f64b8af184aeb8bc1035af66c70ea
Source noteuspto-grants-1983_08